A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610093



Internal ID20983164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:114416901..114418200hg38UCSC Ensembl
chr7:114056956..114058255hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18149267
Samples
Known GenesFOXP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610093
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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