A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021807



Internal ID19111025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:114602745..114669440hg38UCSC Ensembl
Innerchr5:113938442..114005137hg19UCSC Ensembl
Innerchr5:113966341..114033036hg18UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3866696
hg1966696
hg1866696
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5786n100
Supporting Variantsnssv3746587
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)nsv1021807
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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