A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17498085



Internal ID22556019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:67818620..67875110hg38UCSC Ensembl
chr5:67114448..67170938hg19UCSC Ensembl
Cytoband5q13.1
Allele length
AssemblyAllele length
hg3856491
hg1956491
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5843458
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17498085
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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