A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6395806



Internal ID21053359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:167026560..167239514hg38UCSC Ensembl
chr5:166453565..166666519hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38212955
hg19212955
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216002
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6395806
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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