A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6347383



Internal ID21004936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:83943569..83954764hg38UCSC Ensembl
chr2:84170693..84181888hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg3811196
hg1911196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18092175
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6347383
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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