A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612554



Internal ID6999454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23860130..23865015hg38UCSC Ensembl
Innerchr7:23860150..23864996hg38UCSC Ensembl
Outerchr7:23860111..23865035hg38UCSC Ensembl
chr7:23899749..23904634hg19UCSC Ensembl
Innerchr7:23899769..23904615hg19UCSC Ensembl
Outerchr7:23899730..23904654hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg384886
hg194886
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12704117
SamplesHG03643
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612554
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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