A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv739440



Internal ID15686710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:245473737..245484059hg38UCSC Ensembl
Innerchr1:245637039..245647361hg19UCSC Ensembl
Innerchr1:243703662..243713984hg18UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3810323
hg1910323
hg1810323
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv549508
Supporting Variants
Samples
Known GenesKIF26B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv739440
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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