A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5640683



Internal ID21588988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156671656..156671656hg38UCSC Ensembl
chr7:156464350..156464350hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17154919
SamplesHG03683
Known GenesRNF32
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5640683
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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