A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015642



Internal ID21924985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156219138..156219239hg38UCSC Ensembl
chr7:156011832..156011933hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17574409
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015642
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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