A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891179



Internal ID18838889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:110688548..110977789hg38UCSC Ensembl
Outerchr7:110680188..110980787hg38UCSC Ensembl
Innerchr7:110328604..110617845hg19UCSC Ensembl
Outerchr7:110320244..110620843hg19UCSC Ensembl
Innerchr7:110115840..110405081hg18UCSC Ensembl
Outerchr7:110107480..110408079hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38300600
hg19300600
hg18300600
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787815, essv25791422
Samples
Known GenesIMMP2L
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891179
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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