A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3508258



Internal ID18806539
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 StatusS
Merged Variantsnsv1045454
Supporting Variants
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)nssv3508258
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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