A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524733



Internal ID15452026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:95157354..95184076hg38UCSC Ensembl
Innerchr7:94786666..94813388hg19UCSC Ensembl
Innerchr7:94624602..94651324hg18UCSC Ensembl
Innerchr7:94431317..94458039hg17UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3826723
hg1926723
hg1826723
hg1726723
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700724
Samples
Known GenesPPP1R9A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524733
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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