A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10065



Internal ID15542732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:77515279..77546075hg38UCSC Ensembl
Outerchr15:77807621..77838417hg19UCSC Ensembl
Outerchr15:75594676..75625472hg18UCSC Ensembl
Outerchr15:75594676..75625472hg17UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg388704
hg198704
hg188704
hg178704
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1624
Supporting Variants
SamplesNA18956
Known Genes
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv10065
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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