A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5839971



Internal ID22614906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:56845242..56846441hg38UCSC Ensembl
chr4:57711408..57712607hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17495974, nssv17495975
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5839971
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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