A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6350978



Internal ID21008531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:22114254..22205922hg38UCSC Ensembl
chr2:22337126..22428794hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3891669
hg1991669
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3807n223
Supporting Variantsnssv18086242
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6350978
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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