A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25793044



Internal ID18813159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:64300703..64450069hg38UCSC Ensembl
Innerchr7:63761081..63910447hg19UCSC Ensembl
Innerchr7:63398516..63547882hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38149367
hg19149367
hg18149367
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891131
Supporting Variants
Samples
Known GenesYWHAEP1, ZNF736
MethodSNP array
Analysis
PlatformIllumina HumanHap 550
CommentsNumber of probes=23
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25793044
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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