A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6424291



Internal ID21081844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:17346919..17349019hg38UCSC Ensembl
chr9:17346917..17349017hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg382101
hg192101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18174784
Samples
Known GenesCNTLN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6424291
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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