A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526154



Internal ID15453447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:114942136..114945614hg38UCSC Ensembl
Innerchr7:114582191..114585669hg19UCSC Ensembl
Innerchr7:114369427..114372905hg18UCSC Ensembl
Innerchr7:114176142..114179620hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg383479
hg193479
hg183479
hg173479
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702413
Samples
Known GenesMDFIC
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526154
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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