A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008206



Internal ID19097425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:167544739..167596377hg38UCSC Ensembl
Innerchr2:168401249..168452887hg19UCSC Ensembl
Innerchr2:168109495..168161133hg18UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3851639
hg1951639
hg1851639
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4101n100
Supporting Variantsnssv3729270
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)nsv1008206
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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