A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001831



Internal ID19091048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:245223553..245351437hg38UCSC Ensembl
Innerchr1:245386855..245514739hg19UCSC Ensembl
Innerchr1:243453478..243581362hg18UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38127885
hg19127885
hg18127885
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3705563
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)nsv1001831
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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