A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605618



Internal ID20978689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:148696404..148697531hg38UCSC Ensembl
chr6:149017540..149018667hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg381128
hg191128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141241
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605618
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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