A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7066



Internal ID15552038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:122897616..122942017hg38UCSC Ensembl
OuterchrX:122031469..122075870hg19UCSC Ensembl
OuterchrX:121859150..121903551hg18UCSC Ensembl
OuterchrX:121757004..121801405hg17UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3844402
hg1944402
hg1844402
hg1744402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1865
SamplesNA18555
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)nsv7066
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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