A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5928759



Internal ID22704003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:28228451..28228538hg38UCSC Ensembl
chr15:28473597..28473684hg19UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17375152
Samples
Known GenesHERC2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5928759
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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