A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6002943



Internal ID21912286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:145916270..145931023hg38UCSC Ensembl
chr7:145613363..145628116hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3814754
hg1914754
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17558580
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6002943
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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