A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10697



Internal ID15542101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:11927045..11946151hg38UCSC Ensembl
OuterchrX:11945164..11964270hg19UCSC Ensembl
OuterchrX:11855085..11874191hg18UCSC Ensembl
OuterchrX:11704821..11723927hg17UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3819107
hg1919107
hg1819107
hg1719107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6800
Supporting Variants
SamplesNA18956
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)nssv10697
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer