A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523039



Internal ID20896400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:8499781..8523948hg38UCSC Ensembl
chr18:8499779..8523946hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3824168
hg1924168
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18044319
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523039
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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