A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054192



Internal ID19143411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:37009900..37107580hg38UCSC Ensembl
Innerchr10:37298828..37396508hg19UCSC Ensembl
Innerchr10:37338834..37436514hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3897681
hg1997681
hg1897681
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv708n100
Supporting Variantsnssv3516583
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)nsv1054192
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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