A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18187895



Internal ID20754935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:61317773..61318087hg38UCSC Ensembl
chr15:61609972..61610286hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6508660
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18187895
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00626


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