A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6793



Internal ID15551738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:9581613..9626255hg38UCSC Ensembl
OuterchrX:9549653..9594295hg19UCSC Ensembl
OuterchrX:9509653..9554295hg18UCSC Ensembl
OuterchrX:9359389..9404031hg17UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3844643
hg1944643
hg1844643
hg1744643
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8684
SamplesNA12156
Known GenesTBL1X
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)nsv6793
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