A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17150168



Internal ID21423370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149878839..149879002hg38UCSC Ensembl
chr7:149575928..149576091hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5578316
Supporting Variants
SamplesHG00731
Known GenesATP6V0E2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17150168
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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