A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4740283



Internal ID20516258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:25031729..25031784hg38UCSC Ensembl
chr6:25031957..25032012hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16260202
Samples
Known GenesFAM65B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4740283
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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