A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3822



Internal ID15538549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:115884228..115889476hg38UCSC Ensembl
OuterchrX:115000561..115005809hg19UCSC Ensembl
OuterchrX:114914589..114919837hg18UCSC Ensembl
OuterchrX:114812443..114817691hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3833833
hg1933833
hg1833833
hg1733833
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7050
Supporting Variants
SamplesNA12878
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)nssv3822
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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