A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6841



Internal ID15205105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:28580318..28610714hg38UCSC Ensembl
OuterchrX:28598435..28628831hg19UCSC Ensembl
OuterchrX:28508356..28538752hg18UCSC Ensembl
OuterchrX:28358092..28388488hg17UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg389348
hg199348
hg189348
hg179348
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3773
SamplesNA12878
Known GenesIL1RAPL1
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)nsv6841
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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