A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611717



Internal ID20984788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110720644..110727712hg38UCSC Ensembl
chr6:111041847..111048915hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg387069
hg197069
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18136687
Samples
Known GenesCDK19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611717
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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