A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6810



Internal ID15205071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:14577095..14622216hg38UCSC Ensembl
OuterchrX:14595217..14640338hg19UCSC Ensembl
OuterchrX:14505138..14550259hg18UCSC Ensembl
OuterchrX:14354874..14399995hg17UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3845122
hg1945122
hg1845122
hg1745122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8689
SamplesNA12156
Known GenesGLRA2
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)nsv6810
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