A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571552



Internal ID16012275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:16157132..16167286hg38UCSC Ensembl
Innerchr16:16250989..16261143hg19UCSC Ensembl
Innerchr16:16158490..16168644hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3810155
hg1910155
hg1810155
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv852831
Samples
Known GenesABCC6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571552
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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