A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7092



Internal ID15552067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:131957262..131988608hg38UCSC Ensembl
OuterchrX:131091290..131122636hg19UCSC Ensembl
OuterchrX:130918971..130950317hg18UCSC Ensembl
OuterchrX:130816825..130848171hg17UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg3831347
hg1931347
hg1831347
hg1731347
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8781
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)nsv7092
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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