A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6882



Internal ID15551836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:44732647..44759893hg38UCSC Ensembl
OuterchrX:44591893..44619139hg19UCSC Ensembl
OuterchrX:44476837..44504083hg18UCSC Ensembl
OuterchrX:44348147..44375393hg17UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3810356
hg1910356
hg1810356
hg1710356
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10698
SamplesNA18956
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)nsv6882
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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