A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894089



Internal ID18838257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:145687602..145809105hg38UCSC Ensembl
Outerchr1:145672100..145824903hg38UCSC Ensembl
Innerchr1:145625979..145747463hg19UCSC Ensembl
Outerchr1:145610210..145762959hg19UCSC Ensembl
Innerchr1:144337336..144458820hg18UCSC Ensembl
Outerchr1:144321567..144474316hg18UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg38152804
hg19152750
hg18152750
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796560, essv25796923, essv25796801
Samples
Known GenesCD160, LOC100288142, NBPF10, PDZK1, POLR3C, RNF115
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894089
Frequency
Sample Size3017
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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