A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6402614



Internal ID21060167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:44199322..44200440hg38UCSC Ensembl
chr6:44167059..44168177hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg381119
hg191119
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224429
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6402614
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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