A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18088903



Internal ID20655943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:69806684..69812065hg38UCSC Ensembl
chr2:70033816..70039197hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg385382
hg195382
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6346481
Supporting Variants
Samples
Known GenesANXA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18088903
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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