A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6479120



Internal ID21136673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:61036279..61044305hg38UCSC Ensembl
chr13:61610413..61618439hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg388027
hg198027
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18010360
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6479120
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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