A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530675



Internal ID20904036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:15980101..15985700hg38UCSC Ensembl
chr20:15960746..15966345hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg385600
hg195600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18066477
Samples
Known GenesMACROD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530675
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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