A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6074252



Internal ID21983485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:46310737..46310737hg38UCSC Ensembl
chr7:46350335..46350335hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg381007
hg191007
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17573136
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6074252
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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