A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571024



Internal ID16011747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:760039..797743hg38UCSC Ensembl
Innerchr16:810039..847743hg19UCSC Ensembl
Innerchr16:750040..787744hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3837705
hg1937705
hg1837705
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4827n54
Supporting Variantsnssv1149280
SamplesHGDP00602
Known GenesCHTF18, MIR662, MSLN, RPUSD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571024
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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