A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6076632



Internal ID21985865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156413778..156413778hg38UCSC Ensembl
chr7:156206472..156206472hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38182
hg19182
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17575799
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6076632
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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