A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6396057



Internal ID21053610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41968988..41971817hg38UCSC Ensembl
chr6:41936726..41939555hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg382830
hg192830
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229537
Samples
Known GenesCCND3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6396057
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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