A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229594



Internal ID20796634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:56475101..56485600hg38UCSC Ensembl
chr8:57387660..57398159hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3810500
hg1910500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6424703
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229594
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00043


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