A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6343393



Internal ID21000946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:65672143..65677316hg38UCSC Ensembl
chr2:65899277..65904450hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg385174
hg195174
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089988
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6343393
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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