A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5921078



Internal ID22696301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:96872067..96882570hg38UCSC Ensembl
chr11:96743067..96753570hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3810504
hg1910504
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17353704
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5921078
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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