A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18076363



Internal ID20643403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:12926501..12927000hg38UCSC Ensembl
chr2:13066627..13067126hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6347936
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18076363
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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