A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571810



Internal ID16012533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:29451203..29466752hg38UCSC Ensembl
Innerchr16:29462524..29478073hg19UCSC Ensembl
Innerchr16:29370025..29385574hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3815550
hg1915550
hg1815550
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv855482
Samples
Known GenesBOLA2, BOLA2B, LOC388242, LOC613038, SLX1A, SLX1A-SULT1A3, SLX1B, SLX1B-SULT1A4, SULT1A3, SULT1A4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571810
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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