A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv855478



Internal ID15802748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:28824174..29032129hg38UCSC Ensembl
Innerchr16:28835495..29043450hg19UCSC Ensembl
Innerchr16:28742996..28950951hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38207956
hg19207956
hg18207956
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571805
Supporting Variants
Samples
Known GenesATP2A1, ATXN2L, CD19, LAT, LOC100289092, MIR4517, MIR4721, NFATC2IP, RABEP2, SH2B1, SPNS1, TUFM
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv855478
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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