A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5639683



Internal ID21587988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157689212..157689212hg38UCSC Ensembl
chr6:158110244..158110244hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17151708
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5639683
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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