A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3706214



Internal ID19004495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:105324556..105374322hg38UCSC Ensembl
Innerchr10:107084314..107134080hg19UCSC Ensembl
Innerchr10:107074304..107124070hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3849767
hg1949767
hg1849767
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043548
Supporting Variants
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)nssv3706214
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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