A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521315



Internal ID20894676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75294897..75297914hg38UCSC Ensembl
chr17:73290978..73293995hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg383018
hg193018
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192957
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521315
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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