A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608982



Internal ID20982053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:116807928..116808281hg38UCSC Ensembl
chr6:117129091..117129444hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg38354
hg19354
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18137184
Samples
Known GenesGPRC6A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608982
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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