A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6582



Internal ID15537281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:20064479..20112348hg38UCSC Ensembl
Outerchr14:20532638..20580507hg19UCSC Ensembl
Outerchr14:19602478..19650347hg18UCSC Ensembl
Outerchr14:19602478..19650347hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3847870
hg1947870
hg1847870
hg1747870
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1202
Supporting Variants
SamplesNA12156
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)nssv6582
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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