A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1207



Internal ID15544523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:69541906..69565924hg38UCSC Ensembl
Outerchr14:70008623..70032641hg19UCSC Ensembl
Outerchr14:69078376..69102394hg18UCSC Ensembl
Outerchr14:69078376..69102394hg17UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg3824019
hg1924019
hg1824019
hg1724019
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1334
Supporting Variants
SamplesNA19240
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)nssv1207
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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