A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5924654



Internal ID22699881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:87510082..87510492hg38UCSC Ensembl
chr7:87139398..87139808hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg38411
hg19411
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17432044
Samples
Known GenesABCB1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5924654
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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