A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6470541



Internal ID21128094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61372719..61381165hg38UCSC Ensembl
chr11:61140191..61148637hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg388447
hg198447
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993139
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6470541
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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