A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5627864



Internal ID21576169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:69749843..69749843hg38UCSC Ensembl
chr6:70459735..70459735hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17143977
SamplesHG01596
Known GenesLMBRD1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5627864
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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