A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999505



Internal ID19159042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:45042683..45074771hg38UCSC Ensembl
Innerchr2:45269822..45301910hg19UCSC Ensembl
Innerchr2:45123326..45155414hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3832089
hg1932089
hg1832089
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3581600
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)nsv999505
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer