A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893821



Internal ID19184641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:175553242..176177948hg38UCSC Ensembl
Outerchr3:175553242..176177948hg38UCSC Ensembl
Innerchr3:175271030..175895736hg19UCSC Ensembl
Outerchr3:175271030..175895736hg19UCSC Ensembl
Innerchr3:176753724..177378430hg18UCSC Ensembl
Outerchr3:176753724..177378430hg18UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg38624707
hg19624707
hg18624707
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25798556
Samples
Known GenesNAALADL2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893821
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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