A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023804



Internal ID19113021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:61520009..61680277hg38UCSC Ensembl
Innerchr9:44727847..44888115hg19UCSC Ensembl
Innerchr9:44667843..44828111hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38160269
hg19160269
hg18160269
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7602n100
Supporting Variantsnssv3761482, nssv3695541, nssv3695548, nssv3695543, nssv3695537, nssv3695544, nssv3695552, nssv3695535, nssv3695542, nssv3695550, nssv3761481, nssv3695551, nssv3695549, nssv3695539, nssv3695536, nssv3695538, nssv3695546, nssv3695540, nssv3695545, nssv3695553, nssv3695547, nssv3695554
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)nsv1023804
Frequency
Sample Size11257
Observed Gain21
Observed Loss1
Observed Complex0
Frequencyn/a


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