A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6612968



Internal ID20986039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:127450682..127451247hg38UCSC Ensembl
chr6:127771827..127772392hg19UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg38566
hg19566
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18137677
Samples
Known GenesKIAA0408, SOGA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6612968
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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