A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3600852



Internal ID6641110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:67587810..67588500hg38UCSC Ensembl
Innerchr4:67587881..67588430hg38UCSC Ensembl
Outerchr4:67587740..67588571hg38UCSC Ensembl
chr4:68453528..68454218hg19UCSC Ensembl
Innerchr4:68453599..68454148hg19UCSC Ensembl
Outerchr4:68453458..68454289hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38691
hg19691
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11476731, essv11476732
SamplesNA18597, NA19041
Known GenesSTAP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3600852
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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