A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6339



Internal ID15190839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:66038430..66071411hg38UCSC Ensembl
OuterchrX:65258272..65291253hg19UCSC Ensembl
OuterchrX:65174997..65207978hg18UCSC Ensembl
OuterchrX:65041293..65074274hg17UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg386458
hg196458
hg186458
hg176458
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6934
Supporting Variants
SamplesNA12156
Known GenesVSIG4
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)nssv6339
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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