A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011843



Internal ID19101061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:143759668..143942259hg38UCSC Ensembl
Innerchr1:149254317..149436830hg19UCSC Ensembl
Innerchr1:147520941..147703454hg18UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg38182592
hg19182514
hg18182514
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv413n100
Supporting Variantsnssv3501228, nssv3493077
Samples
Known GenesFCGR1C, LOC388692
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011843
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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