A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6003232



Internal ID21912575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:106121315..106123079hg38UCSC Ensembl
chr7:105761761..105763525hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg381765
hg191765
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17573273
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6003232
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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