A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063024



Internal ID18805555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88707330..89238482hg38UCSC Ensembl
Innerchr16:88773738..89304890hg19UCSC Ensembl
Innerchr16:87301239..87832391hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38531153
hg19531153
hg18531153
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559993
Samples
Known GenesACSF3, APRT, CBFA2T3, CDH15, CDT1, CTU2, GALNS, LINC00304, LOC100289580, LOC400558, MIR4722, PABPN1L, PIEZO1, SLC22A31, TRAPPC2L, ZNF778
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063024
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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