A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6618918



Internal ID20991989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167789969..167804668hg38UCSC Ensembl
chr6:168190649..168205348hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3814700
hg1914700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18139297
Samples
Known GenesC6orf123
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6618918
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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