A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053229



Internal ID19142448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:29050941..29078834hg38UCSC Ensembl
Innerchr10:29339870..29367763hg19UCSC Ensembl
Innerchr10:29379876..29407769hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg3827894
hg1927894
hg1827894
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv699n100
Supporting Variantsnssv3522228
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)nsv1053229
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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