A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863736



Internal ID22638671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39762890..39780002hg38UCSC Ensembl
chr8:39620409..39637521hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3817113
hg1917113
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17506083
Samples
Known GenesADAM2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863736
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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