A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038798



Internal ID19128017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:97356213..97415876hg38UCSC Ensembl
Innerchr13:98008467..98068130hg19UCSC Ensembl
Innerchr13:96806468..96866131hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3859664
hg1959664
hg1859664
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525518
Samples
Known GenesMBNL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038798
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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