A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14104049



Internal ID21274671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:76789144..76867989hg38UCSC Ensembl
InnerchrX:76009569..76088414hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3878846
hg1978846
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114828
Supporting Variants
Samplessample21
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14104049
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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