A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843356



Internal ID22618291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:56191906..56193196hg38UCSC Ensembl
chr5:55487733..55489023hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg381291
hg191291
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17497407, nssv17497408
Samples
Known GenesANKRD55
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843356
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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