A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5883463



Internal ID22658443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:49280989..49283088hg38UCSC Ensembl
chr20:47897526..47899625hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17486097
Samples
Known GenesZFAS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5883463
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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