A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5984484



Internal ID21893827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:6339853..6340078hg38UCSC Ensembl
chr1:6399913..6400138hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg38226
hg19226
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17520017
Samples
Known GenesACOT7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5984484
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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