A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545268



Internal ID16332677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:6490316..6578004hg38UCSC Ensembl
Innerchr1:6550376..6638064hg19UCSC Ensembl
Innerchr1:6472963..6560651hg18UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg3887689
hg1987689
hg1887689
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv709213
Samples
Known GenesNOL9, PLEKHG5, TAS1R1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545268
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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