A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6461703



Internal ID21119256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86195608..86201452hg38UCSC Ensembl
chr11:85906650..85912494hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg385845
hg195845
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994599
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6461703
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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