A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17500385



Internal ID22558322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:85864652..85887289hg38UCSC Ensembl
chr5:85160470..85183107hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3822638
hg1922638
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5843543
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17500385
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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