A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051994



Internal ID19141213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:8658738..8677909hg38UCSC Ensembl
Innerchr10:8700701..8719872hg19UCSC Ensembl
Innerchr10:8740707..8759878hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3819172
hg1919172
hg1819172
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv669n100
Supporting Variantsnssv3500348, nssv3485173, nssv3494999, nssv3487324, nssv3497644, nssv3498782, nssv3494829, nssv3490690, nssv3487998
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)nsv1051994
Frequency
Sample Size11257
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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