A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002166



Internal ID19091383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:192511045..192569494hg38UCSC Ensembl
Innerchr2:193375771..193434220hg19UCSC Ensembl
Innerchr2:193084016..193142465hg18UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg3858450
hg1958450
hg1858450
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4138n100
Supporting Variantsnssv3583902
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)nsv1002166
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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