A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544195



Internal ID20917434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56725085..56737922hg38UCSC Ensembl
chr20:55300141..55312978hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg3812838
hg1912838
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18070448
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544195
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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