A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14098215



Internal ID21284062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:84688892..84690590hg38UCSC Ensembl
Innerchr1:85154575..85156273hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg381699
hg191699
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110929
Supporting Variants
Samplessample357
Known GenesSSX2IP
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14098215
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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