A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7131



Internal ID15552110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:144300203..144331463hg38UCSC Ensembl
OuterchrX:143383328..143414587hg19UCSC Ensembl
OuterchrX:143211014..143242273hg18UCSC Ensembl
OuterchrX:143108868..143140127hg17UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg3831261
hg1931260
hg1831260
hg1731260
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1876
SamplesNA18555
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)nsv7131
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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