A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8783



Internal ID15535081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:133077261..133121897hg38UCSC Ensembl
OuterchrX:132211289..132255925hg19UCSC Ensembl
OuterchrX:132038955..132083591hg18UCSC Ensembl
OuterchrX:131936809..131981445hg17UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg3844637
hg1944637
hg1844637
hg1744637
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7097
Supporting Variants
SamplesNA12156
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)nssv8783
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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