A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15703170



Internal ID21375446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:99149132..99149447hg38UCSC Ensembl
chr4:100070289..100070604hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4391351
Supporting Variants
Samples
Known GenesLOC100507053
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15703170
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.971264


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