A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890959



Internal ID19185355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:191898950..192071446hg38UCSC Ensembl
Outerchr1:191898950..192071446hg38UCSC Ensembl
Innerchr1:191868080..192040576hg19UCSC Ensembl
Outerchr1:191868080..192040576hg19UCSC Ensembl
Innerchr1:190134703..190307199hg18UCSC Ensembl
Outerchr1:190134703..190307199hg18UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg38172497
hg19172497
hg18172497
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779904
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890959
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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