A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10695



Internal ID15542103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:9405816..9406846hg38UCSC Ensembl
OuterchrX:9373856..9374886hg19UCSC Ensembl
OuterchrX:9333856..9334886hg18UCSC Ensembl
OuterchrX:9183592..9184622hg17UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg3827667
hg1927667
hg1827667
hg1727667
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6792
Supporting Variants
SamplesNA18956
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)nssv10695
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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