A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8763



Internal ID15535101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:111405067..111439135hg38UCSC Ensembl
OuterchrX:110648295..110682363hg19UCSC Ensembl
OuterchrX:110534951..110569019hg18UCSC Ensembl
OuterchrX:110454440..110488508hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg385364
hg195364
hg185364
hg175364
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7038
Supporting Variants
SamplesNA12156
Known GenesDCX, RNU6-28P
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)nssv8763
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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