A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4736218



Internal ID20512165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:206049271..206055158hg38UCSC Ensembl
chr1:206286213..206292097hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg385888
hg195885
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16261372
Samples
Known GenesC1orf186
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4736218
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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