A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891970



Internal ID18839680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:13438356..13504122hg38UCSC Ensembl
Outerchr1:13438356..13504122hg38UCSC Ensembl
Innerchr1:13764823..13830577hg19UCSC Ensembl
Outerchr1:13764823..13830577hg19UCSC Ensembl
Innerchr1:13637410..13703164hg18UCSC Ensembl
Outerchr1:13637410..13703164hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3865767
hg1965755
hg1865755
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780939
Samples
Known GenesLRRC38
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891970
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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