A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15746821



Internal ID21388573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:256001..383000hg38UCSC Ensembl
chr6:256001..383000hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38127000
hg19127000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4434896
Supporting Variants
SamplesNB08
Known GenesDUSP22
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15746821
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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