A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17414773



Internal ID22472643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:148174121..148174674hg38UCSC Ensembl
chr4:149095272..149095825hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg38554
hg19554
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5900754
Supporting Variants
Samples
Known GenesNR3C2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17414773
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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