A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061681



Internal ID19150900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:23729692..24324358hg38UCSC Ensembl
Innerchr19:23912494..24507160hg19UCSC Ensembl
Innerchr19:23704334..24299000hg18UCSC Ensembl
Cytoband19p11
Allele length
AssemblyAllele length
hg38594667
hg19594667
hg18594667
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3481n100
Supporting Variantsnssv3724332
Samples
Known GenesHAVCR1P1, RPSAP58, ZNF254, ZNF681, ZNF726
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061681
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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