A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv852526



Internal ID15799796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:10399260..10504610hg38UCSC Ensembl
Innerchr16:10493117..10598467hg19UCSC Ensembl
Innerchr16:10400618..10505968hg18UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38105351
hg19105351
hg18105351
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571450
Supporting Variants
Samples
Known GenesATF7IP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv852526
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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