A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17422603



Internal ID22480473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:186071683..186072092hg38UCSC Ensembl
chr3:185789472..185789881hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg38410
hg19410
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5895203
Supporting Variants
Samples
Known GenesETV5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17422603
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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