A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5971636



Internal ID22746571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74639701..74639701hg38UCSC Ensembl
chr15:74932042..74932042hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17379083
Samples
Known GenesEDC3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5971636
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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