A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615726



Internal ID20988797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167651363..167651929hg38UCSC Ensembl
chr6:168052043..168052609hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38567
hg19567
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217059
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615726
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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