A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4740662



Internal ID20516638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:201690222..201690439hg38UCSC Ensembl
chr1:201659350..201659567hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38218
hg19218
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16266468
Samples
Known GenesIPO9-AS1, NAV1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4740662
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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