A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526422



Internal ID15453715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:104977871..104992533hg38UCSC Ensembl
Innerchr7:104618318..104632980hg19UCSC Ensembl
Innerchr7:104405554..104420216hg18UCSC Ensembl
Innerchr7:104212269..104226931hg17UCSC Ensembl
Cytoband7q22.2
Allele length
AssemblyAllele length
hg3814663
hg1914663
hg1814663
hg1714663
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702723
Samples
Known GenesLINC01004
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526422
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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