A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14104094



Internal ID21289923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:7419552..7423903hg38UCSC Ensembl
InnerchrX:7337593..7341944hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg384352
hg194352
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110914
Supporting Variants
Samplessample53
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14104094
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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