A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11390827



Internal ID1006680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:34214098..34349125hg38UCSC Ensembl
Innerchr4:34214116..34349108hg38UCSC Ensembl
Outerchr4:34214081..34349143hg38UCSC Ensembl
chr4:34215720..34350747hg19UCSC Ensembl
Innerchr4:34215738..34350730hg19UCSC Ensembl
Outerchr4:34215703..34350765hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38135028
hg19135028
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3600165
Supporting Variants
SamplesHG00629
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11390827
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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