A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6346412



Internal ID21003965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:195225999..195429838hg38UCSC Ensembl
chr2:196090723..196294562hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg38203840
hg19203840
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4245n223
Supporting Variantsnssv18081881
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6346412
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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