A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8764



Internal ID15188414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:111761020..111806086hg38UCSC Ensembl
OuterchrX:111004248..111049314hg19UCSC Ensembl
OuterchrX:110890904..110935970hg18UCSC Ensembl
OuterchrX:110810393..110855459hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3845067
hg1945067
hg1845067
hg1745067
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7039
Supporting Variants
SamplesNA12156
Known GenesTRPC5
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)nssv8764
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