A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv880



Internal ID15198391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:64248242..64264989hg38UCSC Ensembl
OuterchrX:63468122..63484869hg19UCSC Ensembl
OuterchrX:63384847..63401594hg18UCSC Ensembl
OuterchrX:63251143..63267890hg17UCSC Ensembl
CytobandXq11.1
Allele length
AssemblyAllele length
hg386808
hg196808
hg186808
hg176808
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6929
Supporting Variants
SamplesNA19240
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)nssv880
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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