A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025999



Internal ID19115216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:131025220..131437026hg38UCSC Ensembl
Innerchr4:131946375..132358181hg19UCSC Ensembl
Innerchr4:132165825..132577631hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38411807
hg19411807
hg18411807
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5388n100
Supporting Variantsnssv3639468, nssv3639465, nssv3639467, nssv3639463, nssv3639464, nssv3639466, nssv3639469, nssv3639462, nssv3639470, nssv3743103, nssv3743105, nssv3743104
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025999
Frequency
Sample Size11257
Observed Gain12
Observed Loss0
Observed Complex0
Frequencyn/a


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