A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv752213



Internal ID16046169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86222102..86302046hg38UCSC Ensembl
Innerchr10:87981859..88061803hg19UCSC Ensembl
Innerchr10:87971839..88051783hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3879945
hg1979945
hg1879945
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551773
Supporting Variants
Samples
Known GenesGRID1, MIR346
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv752213
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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