A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871203



Internal ID22646140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:74658940..74678360hg38UCSC Ensembl
chr16:74692838..74712258hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3819421
hg1919421
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473360
Samples
Known GenesMLKL, RFWD3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871203
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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