A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045454



Internal ID19134673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:37223441..37390008hg38UCSC Ensembl
Innerchr10:37512369..37678936hg19UCSC Ensembl
Innerchr10:37552375..37718942hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38166568
hg19166568
hg18166568
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3508258
Samples
Known GenesANKRD30A, LINC00993
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045454
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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