A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010191



Internal ID19099409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:245183669..245221864hg38UCSC Ensembl
Innerchr1:245346971..245385166hg19UCSC Ensembl
Innerchr1:243413594..243451789hg18UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3838196
hg1938196
hg1838196
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3491899
Samples
Known GenesKIF26B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010191
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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