A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891107



Internal ID19185503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:48800799..48838524hg38UCSC Ensembl
Outerchr7:48783558..48842832hg38UCSC Ensembl
Innerchr7:48840395..48878120hg19UCSC Ensembl
Outerchr7:48823154..48882428hg19UCSC Ensembl
Innerchr7:48810941..48848666hg18UCSC Ensembl
Outerchr7:48793700..48852974hg18UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg3859275
hg1959275
hg1859275
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788481, essv25788265, essv25791249, essv25789128, essv25790657, essv25789548, essv25790640
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891107
Frequency
Sample Size3017
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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