A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4757966



Internal ID20533826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:36688482..36688482hg38UCSC Ensembl
chr1:37154083..37154083hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16286244
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4757966
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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