A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9482



Internal ID15193510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:49325554..49326754hg38UCSC Ensembl
OuterchrX:49182017..49183214hg19UCSC Ensembl
OuterchrX:49068961..49070158hg18UCSC Ensembl
OuterchrX:48938388..48939585hg17UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3825404
hg1925404
hg1825404
hg1725404
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6896
Supporting Variants
SamplesNA18517
Known GenesGAGE12J
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)nssv9482
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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