A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517822



Internal ID20891183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:5818138..5818813hg38UCSC Ensembl
chr18:5818137..5818812hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38676
hg19676
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18042315
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517822
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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