A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv914111



Internal ID16208067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:96903568..97049417hg38UCSC Ensembl
Innerchr2:97569305..97715154hg19UCSC Ensembl
Innerchr2:96933032..97078881hg18UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38145850
hg19145850
hg18145850
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv582497
Supporting Variants
Samples
Known GenesFAM178B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv914111
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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