A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532467



Internal ID20905828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76371301..76372200hg38UCSC Ensembl
chr18:74083256..74084155hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18044186
Samples
Known GenesZNF516
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532467
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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