A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6007469



Internal ID21916812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:113961902..114050926hg38UCSC Ensembl
chr7:113601957..113690981hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3889025
hg1989025
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17560095
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6007469
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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