A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060429



Internal ID18802960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20646773..20803497hg38UCSC Ensembl
Innerchr19:20829579..20986303hg19UCSC Ensembl
Innerchr19:20621419..20778143hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38156725
hg19156725
hg18156725
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3467n100
Supporting Variantsnssv3724313, nssv3724311, nssv3570560, nssv3724317, nssv3724316, nssv3724312, nssv3570562, nssv3570561, nssv3724315, nssv3570563, nssv3570559, nssv3724314
Samples
Known GenesZNF626
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060429
Frequency
Sample Size29084
Observed Gain12
Observed Loss0
Observed Complex0
Frequencyn/a


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