A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044439



Internal ID19133658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:14941160..15028134hg38UCSC Ensembl
Innerchr10:14983159..15070133hg19UCSC Ensembl
Innerchr10:15023165..15110139hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3886975
hg1986975
hg1886975
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv678n100
Supporting Variantsnssv3516137
Samples
Known GenesDCLRE1C, MEIG1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044439
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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