A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17412050



Internal ID22469920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:182879541..182884741hg38UCSC Ensembl
chr4:183800694..183805894hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg385201
hg195201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5900085
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17412050
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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