A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612610



Internal ID6999510
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12709455, essv12709462, essv12709457, essv12709463, essv12709452, essv12709453, essv12709461, essv12709459, essv12709456, essv12709458, essv12709454, essv12709460
SamplesHG01986, HG02944, NA20853, HG02433, HG02419, HG03199, HG01882, NA20126, HG02470, HG02010, HG01912, HG03271
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612610
Frequency
Sample Size2504
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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