A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5635262



Internal ID21583567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:159845843..159845843hg38UCSC Ensembl
chr6:160266875..160266875hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17146978, nssv17152163
SamplesNA12878, HG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5635262
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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