A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6638



Internal ID15537225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:71411654..71423194hg38UCSC Ensembl
Outerchr15:71703993..71715533hg19UCSC Ensembl
Outerchr15:69491047..69502587hg18UCSC Ensembl
Outerchr15:69491047..69502587hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3811541
hg1911541
hg1811541
hg1711541
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1600
Supporting Variants
SamplesNA12156
Known GenesTHSD4
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)nssv6638
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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