A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17536981



Internal ID21861336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:113979756..113979827hg38UCSC Ensembl
chr2:114737333..114737404hg19UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5985620
Supporting Variants
Samples
Known GenesLOC100499194, LOC440900
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17536981
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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