A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3613858



Internal ID6654066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:80401473..80450329hg38UCSC Ensembl
chr7:80030789..80079645hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3848857
hg1948857
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1305e214
Supporting Variantsessv12861222
SamplesHG02658
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3613858
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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