A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514908



Internal ID20888263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5707844..5733999hg38UCSC Ensembl
chr17:5611164..5637319hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3826156
hg1926156
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190718
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514908
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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