A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv665617



Internal ID15055583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:143921485..144000454hg38UCSC Ensembl
Innerchr4:144842638..144921607hg19UCSC Ensembl
Innerchr4:145062088..145141057hg18UCSC Ensembl
Innerchr4:145200243..145279212hg17UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3878970
hg1978970
hg1878970
hg1778970
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517006
Supporting Variants
Samples
Known GenesGYPB
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv665617
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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