A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6828



Internal ID15551776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:20491692..20515721hg38UCSC Ensembl
OuterchrX:20509810..20533839hg19UCSC Ensembl
OuterchrX:20419731..20443760hg18UCSC Ensembl
OuterchrX:20269467..20293496hg17UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg3813552
hg1913552
hg1813552
hg1713552
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9478
SamplesNA18517
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)nsv6828
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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