A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3489528



Internal ID19077169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:26861..113464hg38UCSC Ensembl
Innerchr10:72797..159404hg19UCSC Ensembl
Innerchr10:62797..149404hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3886604
hg1986608
hg1886608
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1045283
Supporting Variants
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)nssv3489528
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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