A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5626580



Internal ID21574885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:87626748..87626748hg38UCSC Ensembl
chr7:87256064..87256064hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg38275
hg19275
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17152948, nssv17154535
SamplesHG00512, NA24385
Known GenesABCB1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5626580
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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