A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5839688



Internal ID22614623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:55796554..55802595hg38UCSC Ensembl
chr4:56662720..56668761hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg386042
hg196042
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17495957
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5839688
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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