A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610025



Internal ID20983096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:114570193..114570664hg38UCSC Ensembl
chr7:114210248..114210719hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38472
hg19472
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18149875
Samples
Known GenesFOXP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610025
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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