A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3626492



Internal ID18924773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:57189069..57222974hg38UCSC Ensembl
Innerchr4:58055235..58089140hg19UCSC Ensembl
Innerchr4:57749992..57783897hg18UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3833906
hg1933906
hg1833906
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1014829
Supporting Variants
Samples
Known GenesIGFBP7-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3626492
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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