A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4736121



Internal ID20512067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:31780859..31780996hg38UCSC Ensembl
chr1:32246460..32246597hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16263166
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4736121
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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