A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6346057



Internal ID21003610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:181876119..181876435hg38UCSC Ensembl
chr2:182740846..182741162hg19UCSC Ensembl
Cytoband2q31.3
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18080984
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6346057
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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