A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4749610



Internal ID20525642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:145680722..145681509hg38UCSC Ensembl
chr6:146001858..146002645hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg38788
hg19788
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16266214
Samples
Known GenesEPM2A
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4749610
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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