A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5935802



Internal ID22711147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:74752156..74752205hg38UCSC Ensembl
chr18:72464112..72464161hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17391993
Samples
Known GenesZNF407
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5935802
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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