A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6614743



Internal ID20987814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166247687..166248893hg38UCSC Ensembl
chr6:166661175..166662381hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381207
hg191207
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143034
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6614743
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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