A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1429



Internal ID15199306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:102201072..102246584hg38UCSC Ensembl
Outerchr14:102667409..102712921hg19UCSC Ensembl
Outerchr14:101737162..101782674hg18UCSC Ensembl
Outerchr14:101737162..101782674hg17UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3845513
hg1945513
hg1845513
hg1745513
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6610
SamplesNA12156
Known GenesMOK, WDR20
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)nsv1429
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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