A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038343



Internal ID19127562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:29050941..29076222hg38UCSC Ensembl
Innerchr10:29339870..29365151hg19UCSC Ensembl
Innerchr10:29379876..29405157hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg3825282
hg1925282
hg1825282
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv699n100
Supporting Variantsnssv3508462
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)nsv1038343
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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