A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017456



Internal ID19106673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:140024812..140056151hg38UCSC Ensembl
Innerchr4:140945966..140977305hg19UCSC Ensembl
Innerchr4:141165416..141196755hg18UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg3831340
hg1931340
hg1831340
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3641187
Samples
Known GenesMAML3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017456
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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