A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17495908



Internal ID22553841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:52567914..52571998hg38UCSC Ensembl
chr4:53434080..53438164hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg384085
hg194085
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5839957
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17495908
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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