A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6005085



Internal ID21914428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:114557455..114557695hg38UCSC Ensembl
chr7:114197510..114197750hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38241
hg19241
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17566032
Samples
Known GenesFOXP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6005085
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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