A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922161



Internal ID22697386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76961782..76966775hg38UCSC Ensembl
chr11:76672826..76677819hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg384994
hg194994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17364324
Samples
Known GenesACER3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922161
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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