A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6343276



Internal ID21000829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:21792301..21799800hg38UCSC Ensembl
chr2:22015173..22022672hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg387500
hg197500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085865
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6343276
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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