A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527281



Internal ID20900642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:61567730..61576924hg38UCSC Ensembl
chr18:59234963..59244157hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg389195
hg199195
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18043303
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527281
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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