A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014965



Internal ID21924308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:29264778..29269127hg38UCSC Ensembl
chr7:29304394..29308743hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg384350
hg194350
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17575202
Samples
Known GenesCHN2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014965
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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