A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15704094



Internal ID21376370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:167913653..167913730hg38UCSC Ensembl
chr1:167882891..167882968hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4389304
Supporting Variants
Samples
Known GenesADCY10
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15704094
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0402299


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