A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6079753



Internal ID21988986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:7508913..7508913hg38UCSC Ensembl
chr4:7510640..7510640hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38220
hg19220
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17555865
Samples
Known GenesSORCS2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6079753
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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