A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597971



Internal ID6985108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141204893..141211425hg38UCSC Ensembl
Innerchr3:141205393..141210925hg38UCSC Ensembl
Outerchr3:141203893..141212425hg38UCSC Ensembl
chr3:140923735..140930267hg19UCSC Ensembl
Innerchr3:140924235..140929767hg19UCSC Ensembl
Outerchr3:140922735..140931267hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg386533
hg196533
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11163787, essv11163788
SamplesHG03773, HG00182
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597971
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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