A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617083



Internal ID20990154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:115939514..115956904hg38UCSC Ensembl
chr6:116260677..116278067hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg3817391
hg1917391
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18137923
Samples
Known GenesFRK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617083
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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