A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701126



Internal ID15091092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:144623121..144624818hg38UCSC Ensembl
Innerchr7:144320214..144321911hg19UCSC Ensembl
Innerchr7:143951147..143952844hg18UCSC Ensembl
Innerchr7:143757862..143759559hg17UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg381698
hg191698
hg181698
hg171698
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525072
Supporting Variants
Samples
Known GenesTPK1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701126
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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