A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528337



Internal ID20901698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63567058..63570001hg38UCSC Ensembl
chr17:61644419..61647362hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg382944
hg192944
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177949
Samples
Known GenesDCAF7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528337
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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