A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6347188



Internal ID21004741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:162850401..162852500hg38UCSC Ensembl
chr2:163706911..163709010hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18079210
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6347188
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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