A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6614935



Internal ID20988006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:163169638..163174733hg38UCSC Ensembl
chr6:163590670..163595765hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg385096
hg195096
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18142601
Samples
Known GenesPACRG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6614935
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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