A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156832



Internal ID15874738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:52504391..52593195hg38UCSC Ensembl
Innerchr8:53416951..53505755hg19UCSC Ensembl
Innerchr8:53579504..53668308hg18UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg3888805
hg1988805
hg1888805
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611356
Supporting Variants
SamplesHGDP00582
Known GenesFAM150A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156832
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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