A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17499733



Internal ID22557669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:156970472..156971732hg38UCSC Ensembl
chr4:157891624..157892884hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg381261
hg191261
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5838080
Supporting Variants
Samples
Known GenesPDGFC
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17499733
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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