A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462810



Internal ID21120363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34143586..34248365hg38UCSC Ensembl
chr11:34165133..34269912hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38104780
hg19104780
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180796
Samples
Known GenesABTB2, NAT10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6462810
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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