A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6585



Internal ID15190593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:23978492..24022689hg38UCSC Ensembl
Outerchr14:24447701..24491898hg19UCSC Ensembl
Outerchr14:23517541..23561738hg18UCSC Ensembl
Outerchr14:23517541..23561738hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3844198
hg1944198
hg1844198
hg1744198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1217
Supporting Variants
SamplesNA12156
Known GenesDHRS4L1, DHRS4L2
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)nssv6585
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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