A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434084



Internal ID21396086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:71583479..71584384hg38UCSC Ensembl
chr3:71632630..71633535hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38906
hg19906
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15753027
SamplesNB07
Known GenesFOXP1
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434084
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer