A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5632017



Internal ID21580322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73205683..73205683hg38UCSC Ensembl
chr6:73915406..73915406hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17157666
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5632017
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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