A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602023



Internal ID20975094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107915001..107916200hg38UCSC Ensembl
chr6:108236205..108237404hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18136965
Samples
Known GenesSEC63
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602023
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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