A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6346857



Internal ID21004410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:4893584..4902477hg38UCSC Ensembl
chr2:4941174..4950067hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg388894
hg198894
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18086066
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6346857
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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