A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17139279



Internal ID21477885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:99842832..99842955hg38UCSC Ensembl
chr4:100763989..100764112hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5577124
Supporting Variants
SamplesHG03486
Known GenesDAPP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17139279
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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