A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6834



Internal ID15551783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:22959374..22994447hg38UCSC Ensembl
OuterchrX:22977491..23012564hg19UCSC Ensembl
OuterchrX:22887412..22922485hg18UCSC Ensembl
OuterchrX:22737148..22772221hg17UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg384647
hg194647
hg184647
hg174647
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3770
SamplesNA12878
Known GenesLOC100873065
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)nsv6834
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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