A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6902



Internal ID15205172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:49878602..49912339hg38UCSC Ensembl
OuterchrX:49643205..49676946hg19UCSC Ensembl
OuterchrX:49529945..49563686hg18UCSC Ensembl
OuterchrX:49346241..49379982hg17UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg385696
hg195696
hg185696
hg175696
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8720
SamplesNA12156
Known GenesUSP27X, USP27X-AS1
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)nsv6902
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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