A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7045



Internal ID15552015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:115059181..115104078hg38UCSC Ensembl
OuterchrX:114293744..114338641hg19UCSC Ensembl
OuterchrX:114200000..114244897hg18UCSC Ensembl
OuterchrX:114116724..114161621hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3844898
hg1944898
hg1844898
hg1744898
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8767
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)nsv7045
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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