A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011841



Internal ID19101059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:196779623..196932623hg38UCSC Ensembl
Innerchr1:196748753..196901753hg19UCSC Ensembl
Innerchr1:195015376..195168376hg18UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg38153001
hg19153001
hg18153001
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv528n100
Supporting Variantsnssv3493336, nssv3484689, nssv3487056, nssv3501058, nssv3483103, nssv3489033, nssv3484823, nssv3497417
Samples
Known GenesCFHR1, CFHR3, CFHR4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011841
Frequency
Sample Size11257
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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