A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6342474



Internal ID21000027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:53056734..53087049hg38UCSC Ensembl
chr2:53283872..53314187hg19UCSC Ensembl
Cytoband2p16.2
Allele length
AssemblyAllele length
hg3830316
hg1930316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18086828
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6342474
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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