A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6346768



Internal ID21004321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:65744047..65748666hg38UCSC Ensembl
chr2:65971181..65975800hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg384620
hg194620
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089993
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6346768
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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