A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7107



Internal ID15552083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:135799996..135923982hg38UCSC Ensembl
OuterchrX:134933963..135006141hg19UCSC Ensembl
OuterchrX:134761629..134833807hg18UCSC Ensembl
OuterchrX:134659483..134731661hg17UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38123987
hg1972179
hg1872179
hg1772179
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv916, nssv9254
SamplesNA18517, NA19240
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)nsv7107
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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