A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6609



Internal ID15537254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:97399431..97444853hg38UCSC Ensembl
Outerchr14:97865768..97911190hg19UCSC Ensembl
Outerchr14:96935521..96980943hg18UCSC Ensembl
Outerchr14:96935521..96980943hg17UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3845423
hg1945423
hg1845423
hg1745423
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1418
Supporting Variants
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)nssv6609
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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