A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6343663



Internal ID21001216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:59577904..59580189hg38UCSC Ensembl
chr2:59805039..59807324hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg382286
hg192286
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18088762
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6343663
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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