A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6347806



Internal ID21005359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:183603886..183611859hg38UCSC Ensembl
chr2:184468614..184476587hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg387974
hg197974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18081690
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6347806
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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