A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516221



Internal ID20889582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:30005989..30022776hg38UCSC Ensembl
chr18:27585954..27602741hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3816788
hg1916788
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039662
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516221
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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