A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv655244



Internal ID15045210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:188000286..188014029hg38UCSC Ensembl
Innerchr4:188921440..188935183hg19UCSC Ensembl
Innerchr4:189158434..189172177hg18UCSC Ensembl
Innerchr4:189296589..189310332hg17UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg3813744
hg1913744
hg1813744
hg1713744
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519300
Supporting Variants
Samples
Known GenesZFP42
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv655244
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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