A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023765



Internal ID18766298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:100579307..101398051hg38UCSC Ensembl
Innerchr5:99915011..100733755hg19UCSC Ensembl
Innerchr5:99942910..100761654hg18UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg38818745
hg19818745
hg18818745
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3645797
Samples
Known GenesFAM174A, ST8SIA4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023765
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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