A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18136871



Internal ID20703911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:10658700..10676004hg38UCSC Ensembl
chr6:10658933..10676237hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg3817305
hg1917305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6414789
Supporting Variants
Samples
Known GenesC6orf52
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18136871
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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