A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180538



Internal ID20747578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:8160262..8174799hg38UCSC Ensembl
chr10:8202225..8216762hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3814538
hg1914538
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6441481
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180538
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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