A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6020402



Internal ID21929745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:29891128..29891189hg38UCSC Ensembl
chr7:29930744..29930805hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17557883
Samples
Known GenesWIPF3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6020402
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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