A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4735315



Internal ID20511257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:63145078..63145147hg38UCSC Ensembl
chr1:63610749..63610818hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288858
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4735315
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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