A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4735074



Internal ID20511014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:61588982..61589042hg38UCSC Ensembl
chr1:62054654..62054714hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288145
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4735074
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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