A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101813



Internal ID21286794
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 StatusS
Merged Variantsnsv3116329
Supporting Variants
Samplessample394
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101813
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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