A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052886



Internal ID19142105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:2068216..2106060hg38UCSC Ensembl
Innerchr10:2110410..2148254hg19UCSC Ensembl
Innerchr10:2100410..2138254hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3837845
hg1937845
hg1837845
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3502146
Samples
Known GenesMIR6072
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052886
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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