A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17499885



Internal ID22557821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:61632981..61635180hg38UCSC Ensembl
chr5:60928808..60931007hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5843374
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17499885
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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