A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6009962



Internal ID21919305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:157030767..157030950hg38UCSC Ensembl
chr7:156823461..156823644hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17558985
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6009962
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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