A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038046



Internal ID19127265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:55156437..55453930hg38UCSC Ensembl
Innerchr10:56916197..57213690hg19UCSC Ensembl
Innerchr10:56586203..56883696hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38297494
hg19297494
hg18297494
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv865n100
Supporting Variantsnssv3504547
Samples
Known GenesRNU6-59P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038046
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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