A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8744



Internal ID15535120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:75999462..76039548hg38UCSC Ensembl
OuterchrX:75219297..75259383hg19UCSC Ensembl
OuterchrX:75136011..75175776hg18UCSC Ensembl
OuterchrX:75002307..75042072hg17UCSC Ensembl
CytobandXq13.3
Allele length
AssemblyAllele length
hg3840087
hg1940087
hg1839766
hg1739766
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6962
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)nssv8744
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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