A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116329



Internal ID21299595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:93611417..93619159hg38UCSC Ensembl
InnerchrX:92866416..92874158hg19UCSC Ensembl
CytobandXq21.32
Allele length
AssemblyAllele length
hg387743
hg197743
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14101680, nssv14101813, nssv14105043
Samplessample394, sample296, sample197
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116329
Frequency
Sample Size467
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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