A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615727



Internal ID20988798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:142922601..142929600hg38UCSC Ensembl
chr6:143243738..143250737hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg387000
hg197000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216920
Samples
Known GenesHIVEP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615727
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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