A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041009



Internal ID19130228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14956016..15022388hg38UCSC Ensembl
Innerchr16:15049873..15116245hg19UCSC Ensembl
Innerchr16:14957374..15023746hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3866373
hg1966373
hg1866373
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2762n100
Supporting Variantsnssv3557852, nssv3557845, nssv3557846, nssv3557850, nssv3557842, nssv3557848, nssv3557849, nssv3557843, nssv3718974, nssv3718973, nssv3557844, nssv3557851, nssv3557841, nssv3557847, nssv3557853
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)nsv1041009
Frequency
Sample Size11257
Observed Gain1
Observed Loss14
Observed Complex0
Frequencyn/a


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