A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696256



Internal ID15086222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:188100311..188108911hg38UCSC Ensembl
Innerchr4:189021465..189030065hg19UCSC Ensembl
Innerchr4:189258459..189267059hg18UCSC Ensembl
Innerchr4:189396614..189405214hg17UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg388601
hg198601
hg188601
hg178601
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519300
Supporting Variants
Samples
Known GenesTRIML2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696256
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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