A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014345



Internal ID18756879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:180163553..180202226hg38UCSC Ensembl
Innerchr1:180132688..180171361hg19UCSC Ensembl
Innerchr1:178399311..178437984hg18UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg3838674
hg1938674
hg1838674
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv475n100
Supporting Variantsnssv3491580, nssv3490887, nssv3492960, nssv3489223, nssv3486016, nssv3488277, nssv3486231, nssv3500831, nssv3491074
Samples
Known GenesFLJ23867, QSOX1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014345
Frequency
Sample Size29084
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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