A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036256



Internal ID18778787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:90324175..90700158hg38UCSC Ensembl
Innerchr10:92083932..92459915hg19UCSC Ensembl
Innerchr10:92073912..92449895hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38375984
hg19375984
hg18375984
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv952n100
Supporting Variantsnssv3706191
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)nsv1036256
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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