A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10734



Internal ID15195378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:120874010..120990251hg38UCSC Ensembl
OuterchrX:120007864..120124105hg19UCSC Ensembl
OuterchrX:119891892..119951786hg18UCSC Ensembl
OuterchrX:119789746..119849640hg17UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38116242
hg19116242
hg1859895
hg1759895
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7061
Supporting Variants
SamplesNA18956
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)nssv10734
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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