A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17378733



Internal ID22436603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65345237..65346286hg38UCSC Ensembl
chr15:65637575..65638624hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg381050
hg191050
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5940912
Supporting Variants
Samples
Known GenesIGDCC3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17378733
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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