A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170091



Internal ID21314152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:36104694..36112411hg38UCSC Ensembl
Outerchr2:36097392..36123960hg38UCSC Ensembl
Innerchr2:36331837..36339554hg19UCSC Ensembl
Outerchr2:36324535..36351103hg19UCSC Ensembl
Innerchr2:36185341..36193058hg18UCSC Ensembl
Outerchr2:36178039..36204607hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3826569
hg1926569
hg1826569
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14250624, nssv14243900, nssv14242538, nssv14241836, nssv14252471, nssv14242601, nssv14243544, nssv14247388, nssv14242593, nssv14246454, nssv14250687, nssv14241670
SamplesMLY_6, MLY_1, NGO_41, NGO_47, NGO_40, PML_2, NGO_2, NGO_25, MLY_3, MLY_8, NGO_42, NGO_51
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170091
Frequency
Sample Size93
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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