A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019095



Internal ID19108313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:142866890..142880117hg38UCSC Ensembl
Innerchr4:143788043..143801270hg19UCSC Ensembl
Innerchr4:144007493..144020720hg18UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3813228
hg1913228
hg1813228
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5410n100
Supporting Variantsnssv3641193
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)nsv1019095
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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