A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6009002



Internal ID21918345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:47656547..47656923hg38UCSC Ensembl
chr7:47696145..47696521hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg38377
hg19377
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17569692
Samples
Known GenesC7orf65
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6009002
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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