A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4163



Internal ID15538890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:71406634..71425978hg38UCSC Ensembl
Outerchr15:71698973..71718317hg19UCSC Ensembl
Outerchr15:69486027..69505371hg18UCSC Ensembl
Outerchr15:69486027..69505371hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3819345
hg1919345
hg1819345
hg1719345
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1600
Supporting Variants
SamplesNA12878
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)nssv4163
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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