A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5847807



Internal ID22622742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:36388522..36397913hg38UCSC Ensembl
chr8:36246040..36255431hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg389392
hg199392
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2005n209
Supporting Variantsnssv17506013, nssv17506012
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5847807
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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