A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17388932



Internal ID22446802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78300209..78301981hg38UCSC Ensembl
chr15:78592551..78594323hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg381773
hg191773
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5944244
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17388932
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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