A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3530512



Internal ID18828793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:77253900..77280018hg38UCSC Ensembl
Innerchr13:77828035..77854153hg19UCSC Ensembl
Innerchr13:76726036..76752154hg18UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg3826119
hg1926119
hg1826119
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039620
Supporting Variants
Samples
Known GenesMYCBP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3530512
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer