A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2996339



Internal ID15235199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25540816..25708423hg38UCSC Ensembl
Innerchr15:25785963..25953570hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38167608
hg19167608
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv483024
Supporting Variants
Samples
Known GenesATP10A
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nssv2996339
Frequency
Sample Size39
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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