A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614245



Internal ID7001140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97977622..97984367hg38UCSC Ensembl
Innerchr7:97978122..97983867hg38UCSC Ensembl
Outerchr7:97976622..97985367hg38UCSC Ensembl
chr7:97606934..97613679hg19UCSC Ensembl
Innerchr7:97607434..97613179hg19UCSC Ensembl
Outerchr7:97605934..97614679hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg386746
hg196746
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12904478
SamplesNA19030
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614245
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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