A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352940



Internal ID21010493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:108894638..108895021hg38UCSC Ensembl
chr2:109511094..109511477hg19UCSC Ensembl
Cytoband2q12.3
Allele length
AssemblyAllele length
hg38384
hg19384
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18075326
Samples
Known GenesEDAR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352940
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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