A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4751826



Internal ID20527686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:202992025..202992025hg38UCSC Ensembl
chr1:202961153..202961153hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16273380
Samples
Known GenesLOC401980
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4751826
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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