A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025205



Internal ID19114423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:127260952..127415726hg38UCSC Ensembl
Innerchr4:128182107..128336881hg19UCSC Ensembl
Innerchr4:128401557..128556331hg18UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg38154775
hg19154775
hg18154775
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3639426
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)nsv1025205
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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