A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17423404



Internal ID22481274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:61874779..61875106hg38UCSC Ensembl
chr4:62740497..62740824hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5902196
Supporting Variants
Samples
Known GenesLPHN3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17423404
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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