A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467908



Internal ID21125461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62528047..62530429hg38UCSC Ensembl
chr11:62295519..62297901hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg382383
hg192383
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195848
Samples
Known GenesAHNAK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467908
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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