A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052412



Internal ID19141631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:26602016..26672705hg38UCSC Ensembl
Innerchr10:26890945..26961634hg19UCSC Ensembl
Innerchr10:26930951..27001640hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3870690
hg1970690
hg1870690
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv694n100
Supporting Variantsnssv3519236
Samples
Known GenesLINC00202-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052412
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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