A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517613



Internal ID20890974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:55780001..55780700hg38UCSC Ensembl
chr18:53447232..53447931hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18042518
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517613
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