A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354084



Internal ID21011637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:31826997..31864618hg38UCSC Ensembl
chr2:32052066..32089687hg19UCSC Ensembl
Cytoband2p23.1
Allele length
AssemblyAllele length
hg3837622
hg1937622
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085276
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354084
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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