A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17498862



Internal ID22556797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:85342883..85367402hg38UCSC Ensembl
chr5:84638701..84663220hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3824520
hg1924520
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5843782
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17498862
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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