A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2996153



Internal ID15581654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:144812386..144960543hg38UCSC Ensembl
Innerchr7:144509479..144657636hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38148158
hg19148158
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv482916
Supporting Variants
Samples
Known GenesTPK1
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nssv2996153
Frequency
Sample Size39
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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