A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17130033



Internal ID21472701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:56942878..56942878hg38UCSC Ensembl
chr4:57809044..57809044hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38512
hg19512
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5611975
Supporting Variants
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17130033
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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