A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6886



Internal ID15551840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:47167651..47175978hg38UCSC Ensembl
OuterchrX:47027050..47035377hg19UCSC Ensembl
OuterchrX:46911994..46920321hg18UCSC Ensembl
OuterchrX:46783304..46791631hg17UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg388328
hg198328
hg188328
hg178328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8718
SamplesNA12156
Known GenesRBM10
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)nsv6886
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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