A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180446



Internal ID20747486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63789127..63789622hg38UCSC Ensembl
chr17:61866487..61866982hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg38496
hg19496
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6526029
Supporting Variants
Samples
Known GenesDDX42
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180446
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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