A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4742501



Internal ID20518485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:15129248..15129308hg38UCSC Ensembl
chr7:15168873..15168933hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16295523
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4742501
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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