A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6951



Internal ID15551912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:70509208..70528535hg38UCSC Ensembl
OuterchrX:69729058..69748385hg19UCSC Ensembl
OuterchrX:69645783..69665110hg18UCSC Ensembl
OuterchrX:69512079..69531406hg17UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3819328
hg1919328
hg1819328
hg1719328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1845
SamplesNA18555
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)nsv6951
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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