A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5945017



Internal ID22720490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77209292..77282294hg38UCSC Ensembl
chr15:77501634..77574636hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg3873003
hg1973003
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17387171
Samples
Known GenesLINC00597, PEAK1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5945017
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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