A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352114



Internal ID21009667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:65168912..65171843hg38UCSC Ensembl
chr2:65396046..65398977hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg382932
hg192932
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089957
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352114
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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