A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18192449



Internal ID20759490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75111471..75115291hg38UCSC Ensembl
chr17:73107566..73111386hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg383821
hg193821
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6525776
Supporting Variants
Samples
Known GenesARMC7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18192449
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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