A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039590



Internal ID19128809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:12143766..12185717hg38UCSC Ensembl
Innerchr16:12237623..12279574hg19UCSC Ensembl
Innerchr16:12145124..12187075hg18UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3841952
hg1941952
hg1841952
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3557146
Samples
Known GenesSNX29
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039590
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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