A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849062



Internal ID22623997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:43149488..43173732hg38UCSC Ensembl
chr8:43004631..43028875hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3824245
hg1924245
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17506673, nssv17506674
Samples
Known GenesHGSNAT
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849062
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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