A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999870



Internal ID19159406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:108191460..108362858hg38UCSC Ensembl
Innerchr4:109112616..109284014hg19UCSC Ensembl
Innerchr4:109332065..109503463hg18UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38171399
hg19171399
hg18171399
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3743022
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)nsv999870
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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