A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019421



Internal ID19108639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:27891005..27919571hg38UCSC Ensembl
Innerchr8:27748522..27777088hg19UCSC Ensembl
Innerchr8:27804441..27833007hg18UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg3828567
hg1928567
hg1828567
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3685527
Samples
Known GenesSCARA5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019421
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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