A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5942048



Internal ID22717479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64506452..64506502hg38UCSC Ensembl
chr15:64798651..64798701hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17389165
Samples
Known GenesZNF609
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5942048
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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