A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4745874



Internal ID20521885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:91584049..91590556hg38UCSC Ensembl
chr7:91213364..91219871hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg386508
hg196508
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv68n199
Supporting Variantsnssv16287114
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4745874
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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