A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6317



Internal ID15537546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:27964445..28009878hg38UCSC Ensembl
OuterchrX:27982562..28027995hg19UCSC Ensembl
OuterchrX:27892483..27937916hg18UCSC Ensembl
OuterchrX:27742219..27787652hg17UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg3845434
hg1945434
hg1845434
hg1745434
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6839
Supporting Variants
SamplesNA12156
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)nssv6317
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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