A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792701



Internal ID19170138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:67044615..67262802hg38UCSC Ensembl
Innerchr7:66509602..66727789hg19UCSC Ensembl
Innerchr7:66147037..66365224hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38218188
hg19218188
hg18218188
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891138
Supporting Variants
Samples
Known GenesMIR4650-1, MIR4650-2, TYW1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=32
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792701
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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