A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6003827



Internal ID21913170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:8788695..8796428hg38UCSC Ensembl
chr8:8646205..8653938hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg387734
hg197734
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17564677
Samples
Known GenesMFHAS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6003827
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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