A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169971



Internal ID21314032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:187170203..187295023hg38UCSC Ensembl
Outerchr2:187169163..187313374hg38UCSC Ensembl
Innerchr2:188034930..188159750hg19UCSC Ensembl
Outerchr2:188033890..188178101hg19UCSC Ensembl
Innerchr2:187743175..187867995hg18UCSC Ensembl
Outerchr2:187742135..187886346hg18UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg38144212
hg19144212
hg18144212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14251257
SamplesMLY_8
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169971
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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