A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7120



Internal ID15552098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:140410317..140426636hg38UCSC Ensembl
OuterchrX:139492482..139508801hg19UCSC Ensembl
OuterchrX:139320148..139336467hg18UCSC Ensembl
OuterchrX:139218002..139234321hg17UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg3816320
hg1916320
hg1816320
hg1716320
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv920
SamplesNA19240
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)nsv7120
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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