A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549408



Internal ID20922570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56578031..56623899hg38UCSC Ensembl
chr20:55153087..55198955hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg3845869
hg1945869
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4497n223
Supporting Variantsnssv18070429
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549408
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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