A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6461817



Internal ID21119370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65831517..65837618hg38UCSC Ensembl
chr11:65598988..65605089hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg386102
hg196102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17992526
Samples
Known GenesSNX32
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6461817
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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