A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6348809



Internal ID21006362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:16062088..16062421hg38UCSC Ensembl
chr2:16202210..16202543hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18080551
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6348809
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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