A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515737



Internal ID15442794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:128403981..128410363hg38UCSC Ensembl
Innerchr7:128044035..128050417hg19UCSC Ensembl
Innerchr7:127831271..127837653hg18UCSC Ensembl
Innerchr7:127637986..127644368hg17UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg386383
hg196383
hg186383
hg176383
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv682442, nssv677251, nssv664637, nssv670214, nssv682787
Samples
Known GenesIMPDH1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515737
Frequency
Sample Size2026
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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