A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6959



Internal ID15551920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:73891938..73930038hg38UCSC Ensembl
OuterchrX:73111773..73149873hg19UCSC Ensembl
OuterchrX:73028498..73066598hg18UCSC Ensembl
OuterchrX:72894794..72932894hg17UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg3838101
hg1938101
hg1838101
hg1738101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3800
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)nsv6959
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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