A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014900



Internal ID19104117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:209340326..209370838hg38UCSC Ensembl
Innerchr2:210205050..210235562hg19UCSC Ensembl
Innerchr2:209913295..209943807hg18UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3830513
hg1930513
hg1830513
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4162n100
Supporting Variantsnssv3585609
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)nsv1014900
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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