A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514120



Internal ID20887472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15140601..15156700hg38UCSC Ensembl
chr17:15043918..15060017hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3816100
hg1916100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3004n223
Supporting Variantsnssv18034445
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514120
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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