A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007880



Internal ID19097099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:168414178..168439367hg38UCSC Ensembl
Innerchr2:169270688..169295877hg19UCSC Ensembl
Innerchr2:168978934..169004123hg18UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3825190
hg1925190
hg1825190
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4102n100
Supporting Variantsnssv3583013
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)nsv1007880
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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