A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5847693



Internal ID22622628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:81025426..81057329hg38UCSC Ensembl
chr8:81937661..81969564hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3831904
hg1931904
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509993
Samples
Known GenesPAG1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5847693
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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