A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893906



Internal ID19184760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:30810152..30920456hg38UCSC Ensembl
Outerchr4:30810152..30920456hg38UCSC Ensembl
Innerchr4:30811774..30922078hg19UCSC Ensembl
Outerchr4:30811774..30922078hg19UCSC Ensembl
Innerchr4:30420872..30531176hg18UCSC Ensembl
Outerchr4:30420872..30531176hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38110305
hg19110305
hg18110305
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785461
Samples
Known GenesPCDH7
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893906
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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