A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052247



Internal ID19141466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:8658738..8678289hg38UCSC Ensembl
Innerchr10:8700701..8720252hg19UCSC Ensembl
Innerchr10:8740707..8760258hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3819552
hg1919552
hg1819552
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv669n100
Supporting Variantsnssv3493664, nssv3493855, nssv3486379
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)nsv1052247
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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