A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036270



Internal ID18778801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:28275066..28285398hg38UCSC Ensembl
Innerchr10:28563995..28574327hg19UCSC Ensembl
Innerchr10:28604001..28614333hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg3810333
hg1910333
hg1810333
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv697n100
Supporting Variantsnssv3502764
Samples
Known GenesMPP7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036270
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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