A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500601



Internal ID20873829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:14363931..14378015hg38UCSC Ensembl
chr17:14267248..14281332hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3814085
hg1914085
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181741
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500601
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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