A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4732434



Internal ID20508358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156762627..156762752hg38UCSC Ensembl
chr1:156732419..156732544hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16265293
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4732434
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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