A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17420749



Internal ID22478619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:168670448..168670810hg38UCSC Ensembl
chr4:169591599..169591961hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38363
hg19363
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5903363
Supporting Variants
Samples
Known GenesPALLD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17420749
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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