A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17371096



Internal ID22596765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25755582..25761320hg38UCSC Ensembl
chr15:26000729..26006467hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg385739
hg195739
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5938379
Supporting Variants
Samples
Known GenesATP10A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17371096
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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