A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17414162



Internal ID22472032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:167583026..167616032hg38UCSC Ensembl
chr3:167300814..167333820hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3833007
hg1933007
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5893142
Supporting Variants
Samples
Known GenesWDR49
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17414162
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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