A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3589364



Internal ID6629653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:242077013..242088139hg38UCSC Ensembl
Innerchr1:242077163..242087989hg38UCSC Ensembl
Outerchr1:242076863..242088289hg38UCSC Ensembl
chr1:242240315..242251441hg19UCSC Ensembl
Innerchr1:242240465..242251291hg19UCSC Ensembl
Outerchr1:242240165..242251591hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg3811127
hg1911127
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10356137
SamplesHG00982
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3589364
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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