A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101767



Internal ID21284090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:75567342..75596288hg38UCSC Ensembl
InnerchrX:74787177..74816123hg19UCSC Ensembl
CytobandXq13.3
Allele length
AssemblyAllele length
hg3828947
hg1928947
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114319
Supporting Variants
Samplessample357
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101767
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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