A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029509



Internal ID19118728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:98552940..98704468hg38UCSC Ensembl
Innerchr5:97888644..98040172hg19UCSC Ensembl
Innerchr5:97916544..98068072hg18UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38151529
hg19151529
hg18151529
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3747527
Samples
Known GenesRNU2-2P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029509
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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