A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047445



Internal ID18789976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:10789399..11147629hg38UCSC Ensembl
Innerchr10:10831362..11189592hg19UCSC Ensembl
Innerchr10:10871368..11229598hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38358231
hg19358231
hg18358231
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3707689
Samples
Known GenesCELF2, CELF2-AS2, LINC00710, SFTA1P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047445
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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