A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5631808



Internal ID21580113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158169586..158169586hg38UCSC Ensembl
chr6:158590618..158590618hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17155247
SamplesNA20509
Known GenesGTF2H5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5631808
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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