A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5912981



Internal ID22688197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:17439181..17439242hg38UCSC Ensembl
chr11:17460728..17460789hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17353256
Samples
Known GenesABCC8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5912981
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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