A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5609507



Internal ID21557812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:82695012..82695012hg38UCSC Ensembl
chr4:83616165..83616165hg19UCSC Ensembl
Cytoband4q21.22
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17132348
SamplesHG03125
Known GenesSCD5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5609507
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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