A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18097663



Internal ID20664703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:185177801..185178358hg38UCSC Ensembl
chr3:184895589..184896146hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg38558
hg19558
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6357651
Supporting Variants
Samples
Known GenesEHHADH-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18097663
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00063


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