A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033772



Internal ID19122993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:142866890..142879808hg38UCSC Ensembl
Innerchr4:143788043..143800961hg19UCSC Ensembl
Innerchr4:144007493..144020411hg18UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3812919
hg1912919
hg1812919
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5410n100
Supporting Variantsnssv3641192
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)nsv1033772
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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