A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12709459



Internal ID3305440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:25735770..25745383hg38UCSC Ensembl
Innerchr7:25735770..25745383hg38UCSC Ensembl
Outerchr7:25735562..25745611hg38UCSC Ensembl
chr7:25775390..25785003hg19UCSC Ensembl
Innerchr7:25775390..25785003hg19UCSC Ensembl
Outerchr7:25775182..25785231hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg389614
hg199614
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3612610
Supporting Variants
SamplesHG02944
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12709459
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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