A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030291



Internal ID18772822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17216947..17262805hg38UCSC Ensembl
Innerchr9:17216945..17262803hg19UCSC Ensembl
Innerchr9:17206945..17252803hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3845859
hg1945859
hg1845859
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3755813
Samples
Known GenesCNTLN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1030291
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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