A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005210



Internal ID18747741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:3711267..3772212hg38UCSC Ensembl
Innerchr4:3712994..3773939hg19UCSC Ensembl
Innerchr4:3682792..3743737hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg3860946
hg1960946
hg1860946
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3616123
Samples
Known GenesADRA2C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1005210
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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