A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020064



Internal ID19109283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:114082815..114157254hg38UCSC Ensembl
Innerchr5:113418512..113492951hg19UCSC Ensembl
Innerchr5:113446411..113520850hg18UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3874440
hg1974440
hg1874440
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3746583
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)nsv1020064
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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