A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862858



Internal ID22637793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:70974577..70981200hg38UCSC Ensembl
chr8:71886812..71893435hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg386624
hg196624
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509790
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862858
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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