A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6009835



Internal ID21919178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:43714640..43720006hg38UCSC Ensembl
chr7:43754239..43759605hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg385367
hg195367
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17573059
Samples
Known GenesCOA1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6009835
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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