A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051774



Internal ID18794305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:19822918..19936310hg38UCSC Ensembl
Innerchr13:20397058..20510450hg19UCSC Ensembl
Innerchr13:19295058..19408450hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38113393
hg19113393
hg18113393
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1609n100
Supporting Variantsnssv3523119
Samples
Known GenesZMYM5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051774
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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