A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3570557



Internal ID18522152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20646773..20797495hg38UCSC Ensembl
Innerchr19:20829579..20980301hg19UCSC Ensembl
Innerchr19:20621419..20772141hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38150723
hg19150723
hg18150723
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1067256
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)nssv3570557
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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