A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15745779



Internal ID21386356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:164930512..164931511hg38UCSC Ensembl
chr6:165344001..165345000hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4434812
Supporting Variants
SamplesMDQ010
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15745779
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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