A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6007939



Internal ID21917282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139225747..139226034hg38UCSC Ensembl
chr7:138910493..138910780hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38288
hg19288
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17559523
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6007939
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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