A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011088



Internal ID19100305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:143417049..143444327hg38UCSC Ensembl
Innerchr3:143135891..143163169hg19UCSC Ensembl
Innerchr3:144618581..144645859hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3827279
hg1927279
hg1827279
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3606127
Samples
Known GenesSLC9A9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011088
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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