A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519043



Internal ID20892404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:31972174..31973949hg38UCSC Ensembl
chr18:29552137..29553912hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg381776
hg191776
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3340n223
Supporting Variantsnssv18039951
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519043
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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