A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413675



Internal ID21071228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:17306297..17313197hg38UCSC Ensembl
chr6:17306528..17313428hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg386901
hg196901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143248
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413675
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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