A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849782



Internal ID22624717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:98074525..98103436hg38UCSC Ensembl
chr8:99086753..99115664hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg3828912
hg1928912
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17510311
Samples
Known GenesC8orf47, HRSP12
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849782
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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