A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856281



Internal ID22631216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39219620..39245111hg38UCSC Ensembl
chr8:39077139..39102630hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3825492
hg1925492
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17506067
Samples
Known GenesADAM32
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856281
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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