A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496917



Internal ID20870120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:7916267..7920509hg38UCSC Ensembl
chr17:7819585..7823827hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg384243
hg194243
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185422
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496917
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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