A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15754012



Internal ID21385253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13021056..13027307hg38UCSC Ensembl
chr6:13021288..13027539hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg386252
hg196252
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4434751
Supporting Variants
SamplesBTQ055
Known GenesPHACTR1
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15754012
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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