A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15706816



Internal ID21379092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:45096288..45096550hg38UCSC Ensembl
chr1:45561960..45562222hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg38263
hg19263
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4390975
Supporting Variants
Samples
Known GenesZSWIM5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15706816
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.152299


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