A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008856



Internal ID19098074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:226227434..226286194hg38UCSC Ensembl
Innerchr2:227092150..227150910hg19UCSC Ensembl
Innerchr2:226800394..226859154hg18UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg3858761
hg1958761
hg1858761
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4177n100
Supporting Variantsnssv3586831
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1008856
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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