A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6903



Internal ID15551859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:49885464..49902630hg38UCSC Ensembl
OuterchrX:49650068..49667237hg19UCSC Ensembl
OuterchrX:49536808..49553977hg18UCSC Ensembl
OuterchrX:49353104..49370273hg17UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3817167
hg1917170
hg1817170
hg1717170
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8721
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)nsv6903
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