A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004707



Internal ID21914050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:114462113..114462222hg38UCSC Ensembl
chr7:114102168..114102277hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17566260
Samples
Known GenesFOXP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004707
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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