A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024820



Internal ID18767351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:150442926..151022409hg38UCSC Ensembl
Innerchr4:151364078..151943561hg19UCSC Ensembl
Innerchr4:151583528..152163011hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38579484
hg19579484
hg18579484
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3636076
Samples
Known GenesLRBA, MAB21L2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024820
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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