A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7039



Internal ID15205322
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 StatusM
Merged Variants
Supporting Variantsnssv8764
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)nsv7039
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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