A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3118062



Internal ID21301328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:95038938..95110866hg38UCSC Ensembl
InnerchrX:94293937..94365865hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg3871929
hg1971929
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14104030
Samplessample6
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3118062
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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