A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739852



Internal ID20515828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:61122796..61123320hg38UCSC Ensembl
chr8:62035355..62035879hg19UCSC Ensembl
Cytoband8q12.2
Allele length
AssemblyAllele length
hg38525
hg19525
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16278897
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739852
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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