A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6351036



Internal ID21008589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:36955250..36957960hg38UCSC Ensembl
chr2:37182393..37185103hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg382711
hg192711
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089078
Samples
Known GenesSTRN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6351036
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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