A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5909505



Internal ID22684715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2361679..2361747hg38UCSC Ensembl
chr11:2382909..2382977hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17357602
Samples
Known GenesCD81-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5909505
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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