A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526899



Internal ID20900260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76837061..76841111hg38UCSC Ensembl
chr18:74549017..74553067hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg384051
hg194051
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18044245
Samples
Known GenesZNF236
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526899
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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