A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5930697



Internal ID22705968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:35296788..35296946hg38UCSC Ensembl
chr15:35588989..35589147hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17374805
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5930697
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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