A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11395353



Internal ID5502887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:36512165..36565428hg38UCSC Ensembl
Innerchr4:36512165..36565428hg38UCSC Ensembl
Outerchr4:36511665..36565928hg38UCSC Ensembl
chr4:36513787..36567050hg19UCSC Ensembl
Innerchr4:36513787..36567050hg19UCSC Ensembl
Outerchr4:36513287..36567550hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3853264
hg1953264
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3600231
Supporting Variants
SamplesNA18986
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11395353
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