A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9254



Internal ID15540205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:135831494..135923982hg38UCSC Ensembl
OuterchrX:134948204..135006141hg19UCSC Ensembl
OuterchrX:134775870..134833807hg18UCSC Ensembl
OuterchrX:134673724..134731661hg17UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg3892489
hg1957938
hg1857938
hg1757938
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7107
Supporting Variants
SamplesNA18517
Known GenesCT45A5, 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)nssv9254
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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