A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5878245



Internal ID22653210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62448109..62473518hg38UCSC Ensembl
chr20:61023165..61048574hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3825410
hg1925410
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17487309
Samples
Known GenesGATA5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5878245
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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