A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6612009



Internal ID20985080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107665171..107700761hg38UCSC Ensembl
chr6:107986375..108021965hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3835591
hg1935591
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18136955
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6612009
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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