A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6006262



Internal ID21915605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142302264..142343279hg38UCSC Ensembl
chr7:142002087..142043109hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3841016
hg1941023
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17571369
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6006262
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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