A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602591



Internal ID20975662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:105548169..105548901hg38UCSC Ensembl
chr6:105996044..105996776hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38733
hg19733
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18134711
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602591
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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