A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061083



Internal ID19150302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:31231779..31258443hg38UCSC Ensembl
Innerchr19:31722685..31749349hg19UCSC Ensembl
Innerchr19:36414525..36441189hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3826665
hg1926665
hg1826665
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3566569
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)nsv1061083
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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