A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528236



Internal ID20901597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:77947933..77950481hg38UCSC Ensembl
chr17:75944015..75946563hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg382549
hg192549
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196723
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528236
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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