A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520675



Internal ID20894036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:31131234..31131572hg38UCSC Ensembl
chr18:28711197..28711535hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039895
Samples
Known GenesDSC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520675
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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