A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv907



Internal ID15198071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:120870918..120987646hg38UCSC Ensembl
OuterchrX:120004772..120121500hg19UCSC Ensembl
OuterchrX:119888800..119949181hg18UCSC Ensembl
OuterchrX:119786654..119847035hg17UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38116729
hg19116729
hg1860382
hg1760382
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7061
Supporting Variants
SamplesNA19240
Known GenesCT47A1, CT47A10, CT47A11, CT47A12, CT47A2, CT47A3, CT47A4, CT47A5, CT47A6, CT47A7, CT47A8, CT47A9, CT47B1
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)nssv907
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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