A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18193702



Internal ID20760742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5036238..5044076hg38UCSC Ensembl
chr17:4939533..4947371hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg387839
hg197839
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6500960
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18193702
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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