A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17389165



Internal ID22447035
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 StatusS
Merged Variantsnsv5942048
Supporting Variants
Samples
Known GenesZNF609
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17389165
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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