A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7062



Internal ID15552034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:121877150..121909323hg38UCSC Ensembl
OuterchrX:121011003..121043176hg19UCSC Ensembl
OuterchrX:120838684..120870857hg18UCSC Ensembl
OuterchrX:120736538..120768711hg17UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg387264
hg197264
hg187264
hg177264
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6369
SamplesNA12156
Known Genes
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)nsv7062
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer