A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1311



Internal ID15199188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:64886004..64913084hg38UCSC Ensembl
Outerchr14:65352722..65379802hg19UCSC Ensembl
Outerchr14:64422475..64449555hg18UCSC Ensembl
Outerchr14:64422475..64449555hg17UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3827081
hg1927081
hg1827081
hg1727081
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6597
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)nsv1311
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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