A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014926



Internal ID21924269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:87589803..87589877hg38UCSC Ensembl
chr7:87219119..87219193hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17565736
Samples
Known GenesABCB1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014926
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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