A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11361007



Internal ID2765436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:17177989..17179026hg38UCSC Ensembl
Innerchr4:17178039..17178976hg38UCSC Ensembl
Outerchr4:17177939..17179076hg38UCSC Ensembl
chr4:17179612..17180649hg19UCSC Ensembl
Innerchr4:17179662..17180599hg19UCSC Ensembl
Outerchr4:17179562..17180699hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg381038
hg191038
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3599770
Supporting Variants
SamplesHG02433
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11361007
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