A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14105108



Internal ID21277112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:128218479..128403355hg38UCSC Ensembl
InnerchrX:127352456..127537333hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38184877
hg19184878
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113091
Supporting Variants
Samplessample246
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14105108
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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