A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6612026



Internal ID20985097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:97417185..97421264hg38UCSC Ensembl
chr6:97865061..97869140hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg384080
hg194080
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18150552
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6612026
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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