A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11394155



Internal ID6736005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:35625818..35628520hg38UCSC Ensembl
Innerchr4:35625835..35628504hg38UCSC Ensembl
Outerchr4:35625802..35628537hg38UCSC Ensembl
chr4:35627440..35630142hg19UCSC Ensembl
Innerchr4:35627457..35630126hg19UCSC Ensembl
Outerchr4:35627424..35630159hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg382703
hg192703
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3600197
Supporting Variants
SamplesNA20858
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11394155
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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