A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182176



Internal ID20749216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:7635021..7637877hg38UCSC Ensembl
chr17:7538339..7541195hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg382857
hg192857
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6511764
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182176
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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