A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6343432



Internal ID21000985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:165858896..165859545hg38UCSC Ensembl
chr2:166715406..166716055hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg38650
hg19650
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18081254
Samples
Known GenesLOC100506124
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6343432
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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