A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614154



Internal ID7001049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:92913895..92925905hg38UCSC Ensembl
Innerchr7:92914395..92925405hg38UCSC Ensembl
Outerchr7:92912895..92926905hg38UCSC Ensembl
chr7:92543209..92555219hg19UCSC Ensembl
Innerchr7:92543709..92554719hg19UCSC Ensembl
Outerchr7:92542209..92556219hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg3812011
hg1912011
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12890770
SamplesHG00657
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614154
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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