A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413623



Internal ID21071176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73898320..74114295hg38UCSC Ensembl
chr6:74608036..74824011hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38215976
hg19215976
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222469
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413623
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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