A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061566



Internal ID19150785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35364439..35376040hg38UCSC Ensembl
Innerchr19:35855341..35866942hg19UCSC Ensembl
Innerchr19:40547181..40558782hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3811602
hg1911602
hg1811602
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3522n100
Supporting Variantsnssv3568156, nssv3724514, nssv3568153, nssv3724515, nssv3568155, nssv3568154
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)nsv1061566
Frequency
Sample Size11257
Observed Gain2
Observed Loss4
Observed Complex0
Frequencyn/a


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