A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527340



Internal ID20900701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9869557..9875236hg38UCSC Ensembl
chr18:9869554..9875233hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg385680
hg195680
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18044253
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527340
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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