A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893507



Internal ID18837641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:174421143..174451651hg38UCSC Ensembl
Outerchr2:174421143..174451651hg38UCSC Ensembl
Innerchr2:175285871..175316379hg19UCSC Ensembl
Outerchr2:175285871..175316379hg19UCSC Ensembl
Innerchr2:174994117..175024625hg18UCSC Ensembl
Outerchr2:174994117..175024625hg18UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3830509
hg1930509
hg1830509
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25784799
Samples
Known GenesGPR155, SCRN3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893507
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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