A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11190161



Internal ID6851912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:154985723..155019134hg38UCSC Ensembl
Innerchr3:154985723..155019134hg38UCSC Ensembl
Outerchr3:154985223..155019634hg38UCSC Ensembl
chr3:154703512..154736923hg19UCSC Ensembl
Innerchr3:154703512..154736923hg19UCSC Ensembl
Outerchr3:154703012..154737423hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3833412
hg1933412
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598263
Supporting Variants
SamplesNA21088
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11190161
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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