A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv482916



Internal ID15582284
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 StatusM
Merged Variants
Supporting Variantsnssv2996153
Samples
Known GenesTPK1
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nsv482916
Frequency
Sample Size39
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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