A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6348108



Internal ID21005661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:83549780..83740446hg38UCSC Ensembl
chr2:83776904..83967570hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38190667
hg19190667
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18091550
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6348108
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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