A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033719



Internal ID19122940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:98110505..98221623hg38UCSC Ensembl
Innerchr5:97446209..97557327hg19UCSC Ensembl
Innerchr5:97471965..97583083hg18UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38111119
hg19111119
hg18111119
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3640468
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033719
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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