A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6586



Internal ID15190592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:24004090..24035741hg38UCSC Ensembl
Outerchr14:24473299..24504950hg19UCSC Ensembl
Outerchr14:23543139..23574790hg18UCSC Ensembl
Outerchr14:23543139..23574790hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3831652
hg1931652
hg1831652
hg1731652
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)nssv6586
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer