A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893995



Internal ID19184849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:97548800..97952516hg38UCSC Ensembl
Outerchr4:97548800..97952516hg38UCSC Ensembl
Innerchr4:98469951..98873667hg19UCSC Ensembl
Outerchr4:98469951..98873667hg19UCSC Ensembl
Innerchr4:98688974..99092690hg18UCSC Ensembl
Outerchr4:98688974..99092690hg18UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg38403717
hg19403717
hg18403717
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789231
Samples
Known GenesSTPG2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893995
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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