A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1858



Internal ID15194456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:115265094..115300490hg38UCSC Ensembl
OuterchrX:114499665..114535056hg19UCSC Ensembl
OuterchrX:114405921..114441312hg18UCSC Ensembl
OuterchrX:114322645..114358036hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3835397
hg1935392
hg1835392
hg1735392
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7046
Supporting Variants
SamplesNA18555
Known GenesLUZP4
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)nssv1858
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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