A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6007078



Internal ID21916421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:77911193..77911247hg38UCSC Ensembl
chr7:77540510..77540564hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17575142
Samples
Known GenesPHTF2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6007078
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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