A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000226



Internal ID19089443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:6156632..6241803hg38UCSC Ensembl
Innerchr3:6198319..6283490hg19UCSC Ensembl
Innerchr3:6173319..6258490hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3885172
hg1985172
hg1885172
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3591699
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)nsv1000226
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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