A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612560



Internal ID6999460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:24014233..24017544hg38UCSC Ensembl
Innerchr7:24014237..24017540hg38UCSC Ensembl
Outerchr7:24014229..24017548hg38UCSC Ensembl
chr7:24053852..24057163hg19UCSC Ensembl
Innerchr7:24053856..24057159hg19UCSC Ensembl
Outerchr7:24053848..24057167hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg383312
hg193312
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12706628
SamplesNA20798
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612560
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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