A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891115



Internal ID18838825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:212828746..212857815hg38UCSC Ensembl
Outerchr1:212828746..212857815hg38UCSC Ensembl
Innerchr1:213002088..213031157hg19UCSC Ensembl
Outerchr1:213002088..213031157hg19UCSC Ensembl
Innerchr1:211068711..211097780hg18UCSC Ensembl
Outerchr1:211068711..211097780hg18UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg3829070
hg1929070
hg1829070
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796216
Samples
Known GenesC1orf227, FLVCR1-AS1
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891115
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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