A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440290



Internal ID21097843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:6412403..6413723hg38UCSC Ensembl
chr11:6433633..6434953hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381321
hg191321
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187199
Samples
Known GenesAPBB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440290
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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