A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434751



Internal ID21396753
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 StatusM
Merged Variants
Supporting Variantsnssv15750712, nssv15754012
SamplesBTQ038, BTQ055
Known GenesPHACTR1
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434751
Frequency
Sample Size15
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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