A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150506



Internal ID15507818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6996257..7044206hg38UCSC Ensembl
Innerchr16:7046258..7094207hg19UCSC Ensembl
Innerchr16:6986259..7034208hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3847950
hg1947950
hg1847950
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571388
Supporting Variants
Samples1780862176_A
Known GenesRBFOX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150506
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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