A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528077



Internal ID15455370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:144736254..144753576hg38UCSC Ensembl
Innerchr7:144433347..144450669hg19UCSC Ensembl
Innerchr7:144064280..144081602hg18UCSC Ensembl
Innerchr7:143870995..143888317hg17UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3817323
hg1917323
hg1817323
hg1717323
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704613
Samples
Known GenesTPK1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528077
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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