A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6813



Internal ID15205074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:15339080..15383961hg38UCSC Ensembl
OuterchrX:15357202..15402083hg19UCSC Ensembl
OuterchrX:15267123..15312004hg18UCSC Ensembl
OuterchrX:15116859..15161740hg17UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3844882
hg1944882
hg1844882
hg1744882
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8691
SamplesNA12156
Known GenesFIGF, PIR-FIGF
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)nsv6813
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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