A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527105



Internal ID15454398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:104185554..104195684hg38UCSC Ensembl
Innerchr7:103826002..103836132hg19UCSC Ensembl
Innerchr7:103613238..103623368hg18UCSC Ensembl
Innerchr7:103419953..103430083hg17UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3810131
hg1910131
hg1810131
hg1710131
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703485
Samples
Known GenesORC5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527105
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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