A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048831



Internal ID18791362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:3749938..3783151hg38UCSC Ensembl
Innerchr10:3792130..3825343hg19UCSC Ensembl
Innerchr10:3782130..3815343hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3833214
hg1933214
hg1833214
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv661n100
Supporting Variantsnssv3492483
Samples
Known GenesKLF6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048831
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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