A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019980



Internal ID19109199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:143429422..143478783hg38UCSC Ensembl
Innerchr4:144350575..144399936hg19UCSC Ensembl
Innerchr4:144570025..144619386hg18UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3849362
hg1949362
hg1849362
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3641199
Samples
Known GenesGAB1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019980
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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