A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053398



Internal ID19142617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:59030368..59069517hg38UCSC Ensembl
Innerchr10:60790128..60829277hg19UCSC Ensembl
Innerchr10:60460134..60499283hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3839150
hg1939150
hg1839150
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv878n100
Supporting Variantsnssv3522426
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)nsv1053398
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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