A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035039



Internal ID19124258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:166534425..166600690hg38UCSC Ensembl
Innerchr4:167455577..167521841hg19UCSC Ensembl
Innerchr4:167675027..167741291hg18UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3866266
hg1966265
hg1866265
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3634174
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)nsv1035039
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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