A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2077



Internal ID15541360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:66212285..66256966hg38UCSC Ensembl
Outerchr14:66679003..66723684hg19UCSC Ensembl
Outerchr14:65748756..65793437hg18UCSC Ensembl
Outerchr14:65748756..65793437hg17UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3844682
hg1944682
hg1844682
hg1744682
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1314
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)nssv2077
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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