A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760264



Internal ID20536124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32284259..32284259hg38UCSC Ensembl
chr1:32749860..32749860hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288548
Samples
Known GenesLCK
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760264
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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