A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17419539



Internal ID22477409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:6299548..6299742hg38UCSC Ensembl
chr4:6301275..6301469hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38195
hg19195
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5902425
Supporting Variants
Samples
Known GenesWFS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17419539
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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