A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6347862



Internal ID21005415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:39580022..39604014hg38UCSC Ensembl
chr2:39807162..39831154hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg3823993
hg1923993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18086447
Samples
Known GenesLOC728730
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6347862
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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