A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545360



Internal ID15986083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:9261182..9336601hg38UCSC Ensembl
Innerchr1:9321241..9396660hg19UCSC Ensembl
Innerchr1:9243828..9319247hg18UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3875420
hg1975420
hg1875420
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv97n54
Supporting Variantsnssv1173663
Samples1780862066_A
Known GenesH6PD, SPSB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545360
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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