A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045830



Internal ID19135049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14964489..15022388hg38UCSC Ensembl
Innerchr16:15058346..15116245hg19UCSC Ensembl
Innerchr16:14965847..15023746hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3857900
hg1957900
hg1857900
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2762n100
Supporting Variantsnssv3557935, nssv3557929, nssv3557933, nssv3557934, nssv3557932, nssv3557930, nssv3557931
Samples
Known GenesMIR1972-1, MIR1972-2, PDXDC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045830
Frequency
Sample Size11257
Observed Gain1
Observed Loss6
Observed Complex0
Frequencyn/a


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