A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012319



Internal ID19101537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:72871735..73081403hg38UCSC Ensembl
Innerchr1:73337418..73547086hg19UCSC Ensembl
Innerchr1:73110006..73319674hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38209669
hg19209669
hg18209669
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3474358
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)nsv1012319
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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