A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv916



Internal ID15544827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:135799996..135908726hg38UCSC Ensembl
OuterchrX:134933963..134990885hg19UCSC Ensembl
OuterchrX:134761629..134818551hg18UCSC Ensembl
OuterchrX:134659483..134716405hg17UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38108731
hg1956923
hg1856923
hg1756923
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7107
Supporting Variants
SamplesNA19240
Known GenesCT45A4, CT45A5, CT45A6, SAGE1
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)nssv916
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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