A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5623716



Internal ID21572021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:49043637..49043637hg38UCSC Ensembl
chr4:49045654..49045654hg19UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17121324
SamplesHG02587
Known GenesCWH43
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5623716
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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