A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701332



Internal ID15437984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:139739238..139742467hg38UCSC Ensembl
Innerchr4:140660392..140663621hg19UCSC Ensembl
Innerchr4:140879842..140883071hg18UCSC Ensembl
Innerchr4:141017997..141021226hg17UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg383230
hg193230
hg183230
hg173230
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525242
Supporting Variants
Samples
Known GenesMAML3, MGST2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701332
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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