A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15751689



Internal ID21391592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:57436203..60640253hg38UCSC Ensembl
chr6:57301001..57608000hg19UCSC Ensembl
Cytoband6p11.2
Allele length
AssemblyAllele length
hg383204051
hg19307000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4434996
Supporting Variants
SamplesSMI018
Known GenesPRIM2
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15751689
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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