A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101734



Internal ID21282516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:22584623..22676501hg38UCSC Ensembl
InnerchrX:22602740..22694618hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg3891879
hg1991879
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110870
Supporting Variants
Samplessample328
Known GenesLOC100873065
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101734
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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