A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603789



Internal ID20976860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107957401..107958100hg38UCSC Ensembl
chr6:108278605..108279304hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18136971
Samples
Known GenesSEC63
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603789
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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