A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17128583



Internal ID21472675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:139029001..139029001hg38UCSC Ensembl
chr4:139950155..139950155hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5617419
Supporting Variants
SamplesHG03371
Known GenesCCRN4L
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17128583
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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