A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv851



Internal ID15544869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:11929309..11972292hg38UCSC Ensembl
OuterchrX:11947428..11990411hg19UCSC Ensembl
OuterchrX:11857349..11900332hg18UCSC Ensembl
OuterchrX:11707085..11750068hg17UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3842984
hg1942984
hg1842984
hg1742984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6800
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)nssv851
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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