A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178566



Internal ID20745606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5602987..5667703hg38UCSC Ensembl
chr10:5644950..5709666hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3864717
hg1964717
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6437223
Supporting Variants
Samples
Known GenesASB13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178566
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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