A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17383083



Internal ID22440953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25770140..25770192hg38UCSC Ensembl
chr15:26015287..26015339hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5939108
Supporting Variants
Samples
Known GenesATP10A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17383083
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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