A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17499666



Internal ID22557602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:148147638..148148737hg38UCSC Ensembl
chr4:149068789..149069888hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5838056
Supporting Variants
Samples
Known GenesNR3C2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17499666
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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