A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603442



Internal ID20976513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108304070..108319755hg38UCSC Ensembl
chr6:108625274..108640959hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3815686
hg1915686
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18136986
Samples
Known GenesLACE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603442
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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