A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101691



Internal ID21280987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:6537937..7060241hg38UCSC Ensembl
InnerchrX:6455978..6978282hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38522305
hg19522305
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114109
Supporting Variants
Samplessample304
Known GenesHDHD1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101691
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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