A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018344



Internal ID19107561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:113055254..113123156hg38UCSC Ensembl
Innerchr5:112390951..112458853hg19UCSC Ensembl
Innerchr5:112418850..112486752hg18UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg3867903
hg1967903
hg1867903
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3647058
Samples
Known GenesMCC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018344
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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