A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5629358



Internal ID21577663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:71375133..71375133hg38UCSC Ensembl
chr6:72084836..72084836hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17144451, nssv17153788
SamplesHG00512, NA20847
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5629358
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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