A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611822



Internal ID6998725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:1754230..1787747hg38UCSC Ensembl
Innerchr7:1754230..1787747hg38UCSC Ensembl
Outerchr7:1754081..1787900hg38UCSC Ensembl
chr7:1793866..1827383hg19UCSC Ensembl
Innerchr7:1793866..1827383hg19UCSC Ensembl
Outerchr7:1793717..1827536hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3833518
hg1933518
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12666955
SamplesHG02131
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611822
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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