A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5919826



Internal ID22695049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:41503215..41504146hg38UCSC Ensembl
chr8:41360734..41361665hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38932
hg19932
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17437898
Samples
Known GenesGOLGA7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5919826
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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