A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527321



Internal ID15454614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:116994994..117020749hg38UCSC Ensembl
Innerchr7:116635048..116660803hg19UCSC Ensembl
Innerchr7:116422284..116448039hg18UCSC Ensembl
Innerchr7:116228999..116254754hg17UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg3825756
hg1925756
hg1825756
hg1725756
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703746
Samples
Known GenesMIR6132, ST7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527321
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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