A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25784799



Internal ID18813631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:174421143..174451651hg38UCSC Ensembl
Innerchr2:175285871..175316379hg19UCSC Ensembl
Innerchr2:174994117..175024625hg18UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3830509
hg1930509
hg1830509
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893507
Supporting Variants
Samples
Known GenesGPR155, SCRN3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25784799
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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