A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6963



Internal ID15551925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:76702586..76734131hg38UCSC Ensembl
OuterchrX:75922989..75954556hg19UCSC Ensembl
OuterchrX:75839393..75870960hg18UCSC Ensembl
OuterchrX:75705689..75737256hg17UCSC Ensembl
CytobandXq13.3
Allele length
AssemblyAllele length
hg387872
hg197872
hg187872
hg177872
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6344
SamplesNA12156
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)nsv6963
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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