A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18089083



Internal ID20656123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:37032710..37034610hg38UCSC Ensembl
chr2:37259853..37261753hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg381901
hg191901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6339320
Supporting Variants
Samples
Known GenesHEATR5B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18089083
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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