A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530953



Internal ID20904314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:40468774..40604074hg38UCSC Ensembl
chr18:38048738..38184038hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg38135301
hg19135301
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177256
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530953
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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