A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062843



Internal ID19152062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:19596411..19634157hg38UCSC Ensembl
Innerchr17:19499724..19537470hg19UCSC Ensembl
Innerchr17:19440316..19478062hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3837747
hg1937747
hg1837747
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3117n100
Supporting Variantsnssv3719986, nssv3560655, nssv3560673, nssv3560658, nssv3560657, nssv3560659, nssv3560662, nssv3560656, nssv3560654, nssv3719987, nssv3560667, nssv3560661, nssv3560669, nssv3560676, nssv3560675, nssv3560671, nssv3560674, nssv3560670, nssv3560663, nssv3560660, nssv3719985, nssv3560666, nssv3560672, nssv3719984, nssv3560668, nssv3560664, nssv3560665
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062843
Frequency
Sample Size11257
Observed Gain0
Observed Loss27
Observed Complex0
Frequencyn/a


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