A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5609435



Internal ID21557740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:69938702..69938702hg38UCSC Ensembl
chr4:70804420..70804420hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17138412
SamplesHG01114
Known GenesCSN1S1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5609435
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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