A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18089074



Internal ID20656114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:36924201..37188000hg38UCSC Ensembl
chr2:37151344..37415143hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg38263800
hg19263800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6341850
Supporting Variants
Samples
Known GenesEIF2AK2, GPATCH11, HEATR5B, STRN, SULT6B1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18089074
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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