A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041943



Internal ID19131162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:26861..115453hg38UCSC Ensembl
Innerchr10:72797..161393hg19UCSC Ensembl
Innerchr10:62797..151393hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3888593
hg1988597
hg1888597
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv646n100
Supporting Variantsnssv3484558, nssv3501855
Samples
Known GenesTUBB8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041943
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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