A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501569



Internal ID20874804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:41622367..41625206hg38UCSC Ensembl
chr17:39778619..39781458hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg382840
hg192840
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035506
Samples
Known GenesKRT17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501569
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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