A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523215



Internal ID20896576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:5040068..5052336hg38UCSC Ensembl
chr18:5040067..5052335hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3812269
hg1912269
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18042190
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523215
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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