A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3625292



Internal ID18923573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:56677005..56697972hg38UCSC Ensembl
Innerchr4:57543171..57564138hg19UCSC Ensembl
Innerchr4:57237928..57258895hg18UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3820968
hg1920968
hg1820968
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv999750
Supporting Variants
Samples
Known GenesHOPX
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3625292
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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