A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6070442



Internal ID21979675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:77814670..77814670hg38UCSC Ensembl
chr7:77443987..77443987hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38167
hg19167
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17574518
Samples
Known GenesPHTF2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6070442
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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