A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv677251



Internal ID15413903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:128403981..128408140hg38UCSC Ensembl
Innerchr7:128044035..128048194hg19UCSC Ensembl
Innerchr7:127831271..127835430hg18UCSC Ensembl
Innerchr7:127637986..127642145hg17UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg384160
hg194160
hg184160
hg174160
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515737
Supporting Variants
Samples
Known GenesIMPDH1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv677251
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer