A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526721



Internal ID15107328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:24576855..24585963hg38UCSC Ensembl
Innerchr7:24616474..24625582hg19UCSC Ensembl
Innerchr7:24582999..24592107hg18UCSC Ensembl
Innerchr7:24389714..24398822hg17UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg389109
hg199109
hg189109
hg179109
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703061
Samples
Known GenesMPP6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526721
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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