A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034748



Internal ID19123969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:189432865..189543091hg38UCSC Ensembl
Innerchr4:190354019..190464245hg19UCSC Ensembl
Innerchr4:190591013..190701239hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38110227
hg19110227
hg18110227
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3636479
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)nsv1034748
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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