A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521979



Internal ID15449272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:130891687..130905032hg38UCSC Ensembl
Innerchr7:130576446..130589791hg19UCSC Ensembl
Innerchr7:130226986..130240331hg18UCSC Ensembl
Innerchr7:130033701..130047046hg17UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3813346
hg1913346
hg1813346
hg1713346
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694746
Samples
Known GenesLOC646329
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521979
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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