A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051096



Internal ID19140315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:20906783..20932747hg38UCSC Ensembl
Innerchr10:21195712..21221676hg19UCSC Ensembl
Innerchr10:21235718..21261682hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3825965
hg1925965
hg1825965
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3513549
Samples
Known GenesNEBL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051096
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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