A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2084



Internal ID15541367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:84811155..84837673hg38UCSC Ensembl
Outerchr14:85277499..85304017hg19UCSC Ensembl
Outerchr14:84347252..84373770hg18UCSC Ensembl
Outerchr14:84347252..84373770hg17UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3826519
hg1926519
hg1826519
hg1726519
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1383
Supporting Variants
SamplesNA18555
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)nssv2084
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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