A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619060



Internal ID20992131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:125794286..125794957hg38UCSC Ensembl
chr6:126115432..126116103hg19UCSC Ensembl
Cytoband6q22.32
Allele length
AssemblyAllele length
hg38672
hg19672
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18138693
Samples
Known GenesNCOA7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619060
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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