A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17422821



Internal ID22480691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:45461295..46225916hg38UCSC Ensembl
chr4:45463312..46227933hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg38764622
hg19764622
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5902470
Supporting Variants
Samples
Known GenesGABRG1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17422821
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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