A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17536871



Internal ID21861226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:39480849..39480949hg38UCSC Ensembl
chr2:39707990..39708090hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5989153
Supporting Variants
Samples
Known GenesLOC728730
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17536871
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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