A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5631196



Internal ID21579501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:70411363..70411363hg38UCSC Ensembl
chr6:71121066..71121066hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17140156
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5631196
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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