A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004476



Internal ID21913819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:144838972..144839050hg38UCSC Ensembl
chr8:146064357..146064435hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585743
Samples
Known GenesZNF7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004476
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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