A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053736



Internal ID19142955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:26861..96453hg38UCSC Ensembl
Innerchr10:72797..142393hg19UCSC Ensembl
Innerchr10:62797..132393hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3869593
hg1969597
hg1869597
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv646n100
Supporting Variantsnssv3707660, nssv3707661, nssv3707659, nssv3497120, nssv3707662, nssv3501232
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)nsv1053736
Frequency
Sample Size11257
Observed Gain1
Observed Loss5
Observed Complex0
Frequencyn/a


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