A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6800



Internal ID15551746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:11907011..11972292hg38UCSC Ensembl
OuterchrX:11925130..11990411hg19UCSC Ensembl
OuterchrX:11835051..11900332hg18UCSC Ensembl
OuterchrX:11684787..11750068hg17UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3865282
hg1965282
hg1865282
hg1765282
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv851, nssv10697, nssv6308, nssv1829
SamplesNA12156, NA18956, NA18555, NA19240
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)nsv6800
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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