A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791422



Internal ID18815090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:110688548..110980787hg38UCSC Ensembl
Innerchr7:110328604..110620843hg19UCSC Ensembl
Innerchr7:110115840..110408079hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38292240
hg19292240
hg18292240
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891179
Supporting Variants
Samples
Known GenesIMMP2L
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=87
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791422
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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