A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17421021



Internal ID22478891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:152782044..152782234hg38UCSC Ensembl
chr4:153703196..153703386hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38191
hg19191
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5892579
Supporting Variants
Samples
Known GenesARFIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17421021
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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