A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608717



Internal ID20981788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:115884401..115893000hg38UCSC Ensembl
chr6:116205565..116214164hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg388600
hg198600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214522
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608717
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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