A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532056



Internal ID20905417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:71565751..71573145hg38UCSC Ensembl
chr17:69561892..69569286hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg387395
hg197395
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178258
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532056
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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