A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6792



Internal ID15551737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:9398354..9425838hg38UCSC Ensembl
OuterchrX:9366394..9393878hg19UCSC Ensembl
OuterchrX:9326394..9353878hg18UCSC Ensembl
OuterchrX:9176130..9203614hg17UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg3813982
hg1913982
hg1813982
hg1713982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv11209, nssv5199, nssv6307, nssv849, nssv10695, nssv1827, nssv3766, nssv9477
SamplesNA12156, NA12878, NA18956, NA15510, NA18555, NA18517, NA19240, NA19129
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)nsv6792
Frequency
Sample Size9
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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