A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1115105



Internal ID15968291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:48169149..48181329hg38UCSC Ensembl
Innerchr8:49081709..49093889hg19UCSC Ensembl
Innerchr8:49244262..49256442hg18UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg3812181
hg1912181
hg1812181
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611307
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1115105
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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