A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv671240



Internal ID15061206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:143921485..143987719hg38UCSC Ensembl
Innerchr4:144842638..144908872hg19UCSC Ensembl
Innerchr4:145062088..145128322hg18UCSC Ensembl
Innerchr4:145200243..145266477hg17UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3866235
hg1966235
hg1866235
hg1766235
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517006
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv671240
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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