A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6342877



Internal ID21000430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:52053301..52057200hg38UCSC Ensembl
chr2:52280439..52284338hg19UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg383900
hg193900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18087979
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6342877
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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