A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6491064



Internal ID21148617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:43832301..43838000hg38UCSC Ensembl
chr13:44406437..44412136hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg385700
hg195700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189542
Samples
Known GenesCCDC122
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6491064
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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