A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6076063



Internal ID21985296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:32531415..32531415hg38UCSC Ensembl
chr7:32571027..32571027hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17558479
Samples
Known GenesAVL9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6076063
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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