A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021237



Internal ID19110455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:61520009..61668092hg38UCSC Ensembl
Innerchr9:44727847..44875930hg19UCSC Ensembl
Innerchr9:44667843..44815926hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38148084
hg19148084
hg18148084
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7602n100
Supporting Variantsnssv3695521, nssv3695527, nssv3695489, nssv3695497, nssv3695481, nssv3695530, nssv3695526, nssv3695513, nssv3695514, nssv3695505, nssv3695471, nssv3695484, nssv3695499, nssv3695522, nssv3695509, nssv3695493, nssv3695524, nssv3761480, nssv3695477, nssv3761472, nssv3695515, nssv3695473, nssv3695534, nssv3695500, nssv3695512, nssv3695510, nssv3761474, nssv3695482, nssv3695488, nssv3695520, nssv3695528, nssv3761473, nssv3695480, nssv3695529, nssv3695479, nssv3695483, nssv3761475, nssv3695475, nssv3695502, nssv3761478, nssv3695511, nssv3761471, nssv3695508, nssv3761477, nssv3695491, nssv3695490, nssv3695518, nssv3695474, nssv3695503, nssv3761479, nssv3695532, nssv3761476, nssv3695517, nssv3695476, nssv3695504, nssv3695507, nssv3695498, nssv3695478, nssv3695501, nssv3695516, nssv3695472, nssv3695525, nssv3695486, nssv3695492, nssv3695469, nssv3695533, nssv3695506, nssv3695470, nssv3695496, nssv3695494, nssv3695531, nssv3695485, nssv3695495, nssv3695487, nssv3695519, nssv3695523
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021237
Frequency
Sample Size11257
Observed Gain72
Observed Loss4
Observed Complex0
Frequencyn/a


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