A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011559



Internal ID19100776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:46190920..46219490hg38UCSC Ensembl
Innerchr2:46418059..46446629hg19UCSC Ensembl
Innerchr2:46271563..46300133hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3828571
hg1928571
hg1828571
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3581624
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)nsv1011559
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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