A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597223



Internal ID6972157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:103355125..103368667hg38UCSC Ensembl
Innerchr3:103355175..103368617hg38UCSC Ensembl
Outerchr3:103355017..103368775hg38UCSC Ensembl
chr3:103073969..103087511hg19UCSC Ensembl
Innerchr3:103074019..103087461hg19UCSC Ensembl
Outerchr3:103073861..103087619hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3813543
hg1913543
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11089180, essv11089181
SamplesNA18999, NA18961
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597223
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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