A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891381



Internal ID18839091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:246962053..247009263hg38UCSC Ensembl
Outerchr1:246962053..247009263hg38UCSC Ensembl
Innerchr1:247125355..247172565hg19UCSC Ensembl
Outerchr1:247125355..247172565hg19UCSC Ensembl
Innerchr1:245191978..245239188hg18UCSC Ensembl
Outerchr1:245191978..245239188hg18UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3847211
hg1947211
hg1847211
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785167
Samples
Known GenesZNF670-ZNF695, ZNF695
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891381
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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