A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5911453



Internal ID22686667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72109926..72110084hg38UCSC Ensembl
chr11:71820972..71821130hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17368017
Samples
Known GenesANAPC15, LRTOMT
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5911453
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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