A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8793



Internal ID15535071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:139733561..139768946hg38UCSC Ensembl
OuterchrX:138815720..138851105hg19UCSC Ensembl
OuterchrX:138643386..138678771hg18UCSC Ensembl
OuterchrX:138541240..138576625hg17UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg3835386
hg1935386
hg1835386
hg1735386
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7116
Supporting Variants
SamplesNA12156
Known GenesATP11C
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)nssv8793
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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