A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17389489



Internal ID22447359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64306297..64307221hg38UCSC Ensembl
chr15:64598496..64599420hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38925
hg19925
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5940955
Supporting Variants
Samples
Known GenesCSNK1G1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17389489
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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