A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6353380



Internal ID21010933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:52370799..52370939hg38UCSC Ensembl
chr2:52597937..52598077hg19UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18086738
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6353380
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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