A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3602480



Internal ID6989514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:142308421..142399449hg38UCSC Ensembl
Innerchr4:142308421..142399449hg38UCSC Ensembl
Outerchr4:142307921..142399949hg38UCSC Ensembl
chr4:143229574..143320602hg19UCSC Ensembl
Innerchr4:143229574..143320602hg19UCSC Ensembl
Outerchr4:143229074..143321102hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3891029
hg1991029
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1031e214
Supporting Variantsessv11636844
SamplesHG02339
Known GenesINPP4B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3602480
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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