A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6365



Internal ID15537498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:115865264..115869140hg38UCSC Ensembl
OuterchrX:114993517..114994408hg19UCSC Ensembl
OuterchrX:114910579..114911465hg18UCSC Ensembl
OuterchrX:114808433..114809319hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3830722
hg1930722
hg1830722
hg1730722
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7050
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)nssv6365
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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