A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11038383



Internal ID4167379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:71786541..71790100hg38UCSC Ensembl
Innerchr3:71786571..71790070hg38UCSC Ensembl
Outerchr3:71786511..71790130hg38UCSC Ensembl
chr3:71835692..71839251hg19UCSC Ensembl
Innerchr3:71835722..71839221hg19UCSC Ensembl
Outerchr3:71835662..71839281hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg383560
hg193560
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3596529
Supporting Variants
SamplesHG03770
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11038383
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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