A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516145



Internal ID20889506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76389628..76408108hg38UCSC Ensembl
chr18:74101584..74120064hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3818481
hg1918481
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18044188
Samples
Known GenesZNF516
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516145
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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