A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3099249



Internal ID11118915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:42409727..42409804hg38UCSC Ensembl
chr7:42449326..42449403hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7368816
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)esv3099249
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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