A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5641308



Internal ID21589613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156264984..156264984hg38UCSC Ensembl
chr7:156057678..156057678hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38495
hg19495
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17158183
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5641308
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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