A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6007047



Internal ID21916390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:19687332..19687644hg38UCSC Ensembl
chr7:19726955..19727267hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17564895
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6007047
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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