A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6396262



Internal ID21053815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:77477832..77611826hg38UCSC Ensembl
chr5:76773657..76907651hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38133995
hg19133995
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5792n223
Supporting Variantsnssv18216621
Samples
Known GenesWDR41
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6396262
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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