A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409163



Internal ID21066716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:76587101..76590000hg38UCSC Ensembl
chr6:77296818..77299717hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg382900
hg192900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6274n223
Supporting Variantsnssv18148210
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409163
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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