A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6345822



Internal ID21003375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:57863353..57863931hg38UCSC Ensembl
chr2:58090488..58091066hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg38579
hg19579
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18088485
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6345822
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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