A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17491071



Internal ID22548996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:8311258..8324661hg38UCSC Ensembl
chr4:8312985..8326388hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3813404
hg1913404
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5840407
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17491071
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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