A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5912568



Internal ID22687784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:37532368..37538068hg38UCSC Ensembl
chr8:37389886..37395586hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg385701
hg195701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17435621
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5912568
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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