A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997458



Internal ID19156994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:55097140..55117190hg38UCSC Ensembl
Innerchr2:55324276..55344326hg19UCSC Ensembl
Innerchr2:55177780..55197830hg18UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3820051
hg1920051
hg1820051
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3849n100
Supporting Variantsnssv3576653
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)nsv997458
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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