A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3724312



Internal ID18675907
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 StatusS
Merged Variantsnsv1060429
Supporting Variants
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)nssv3724312
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer