A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545729



Internal ID16333138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:19657434..19666020hg38UCSC Ensembl
Innerchr1:19983927..19992513hg19UCSC Ensembl
Innerchr1:19856514..19865100hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg388587
hg198587
hg188587
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv711284
Samples
Known GenesHTR6, MINOS1-NBL1, NBL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545729
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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