A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10919



Internal ID15539507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:69535648..69563698hg38UCSC Ensembl
Outerchr14:70002365..70030415hg19UCSC Ensembl
Outerchr14:69072118..69100168hg18UCSC Ensembl
Outerchr14:69072118..69100168hg17UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg3828051
hg1928051
hg1828051
hg1728051
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1334
Supporting Variants
SamplesNA15510
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)nssv10919
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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