A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6839



Internal ID15551788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:27964445..28012816hg38UCSC Ensembl
OuterchrX:27982562..28030933hg19UCSC Ensembl
OuterchrX:27892483..27940854hg18UCSC Ensembl
OuterchrX:27742219..27790590hg17UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg3848372
hg1948372
hg1848372
hg1748372
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5206, nssv6317
SamplesNA12156, NA19129
Known GenesDCAF8L1
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)nsv6839
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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