A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555056



Internal ID20928145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:53542330..53549942hg38UCSC Ensembl
chr20:52158869..52166481hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg387613
hg197613
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067869
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555056
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer