A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169950



Internal ID21314011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:172128078..172165686hg38UCSC Ensembl
Outerchr2:172127288..172172091hg38UCSC Ensembl
Innerchr2:172992806..173030414hg19UCSC Ensembl
Outerchr2:172992016..173036819hg19UCSC Ensembl
Innerchr2:172701052..172738660hg18UCSC Ensembl
Outerchr2:172700262..172745065hg18UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3844804
hg1944804
hg1844804
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14248569, nssv14250091
SamplesSNI_2, SNI_3
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169950
Frequency
Sample Size93
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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