A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6007853



Internal ID21917196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:121648707..121648779hg38UCSC Ensembl
chr7:121288761..121288833hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17567096
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6007853
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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