A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022361



Internal ID18764895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:186346140..188438508hg38UCSC Ensembl
Innerchr4:187267294..189359662hg19UCSC Ensembl
Innerchr4:187504288..189596656hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg382092369
hg192092369
hg182092369
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635634
Samples
Known GenesF11-AS1, FAT1, LOC339975, MTNR1A, TRIML1, TRIML2, ZFP42
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022361
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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