A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526535



Internal ID15453828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:127805540..127983787hg38UCSC Ensembl
Innerchr7:127445594..127623840hg19UCSC Ensembl
Innerchr7:127232830..127411076hg18UCSC Ensembl
Innerchr7:127039545..127217791hg17UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg38178248
hg19178247
hg18178247
hg17178247
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702848
Samples
Known GenesSND1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526535
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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