A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8757



Internal ID15535107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:101802404..101847104hg38UCSC Ensembl
OuterchrX:101057377..101102076hg19UCSC Ensembl
OuterchrX:100944033..100988732hg18UCSC Ensembl
OuterchrX:100863522..100908221hg17UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3844701
hg1944700
hg1844700
hg1744700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7015
Supporting Variants
SamplesNA12156
Known GenesNXF5
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)nssv8757
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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