A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11224



Internal ID15539355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:115883837..115884545hg38UCSC Ensembl
OuterchrX:115000170..115000878hg19UCSC Ensembl
OuterchrX:114914198..114914906hg18UCSC Ensembl
OuterchrX:114812052..114812760hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3835063
hg1935063
hg1835063
hg1735063
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7050
Supporting Variants
SamplesNA15510
Known Genes
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)nssv11224
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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