A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5634056



Internal ID21582361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66383630..66383630hg38UCSC Ensembl
chr7:65848617..65848617hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17154273
SamplesHG03065
Known GenesLINC00174
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5634056
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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