A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890782



Internal ID19185084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:176089646..176167137hg38UCSC Ensembl
Outerchr1:176089646..176167137hg38UCSC Ensembl
Innerchr1:176058782..176136273hg19UCSC Ensembl
Outerchr1:176058782..176136273hg19UCSC Ensembl
Innerchr1:174325405..174402896hg18UCSC Ensembl
Outerchr1:174325405..174402896hg18UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg3877492
hg1977492
hg1877492
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780723
Samples
Known GenesRFWD2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890782
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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