A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044946



Internal ID19134165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:63845046..64363338hg38UCSC Ensembl
Innerchr13:64419179..64937470hg19UCSC Ensembl
Innerchr13:63317180..63835471hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38518293
hg19518292
hg18518292
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1697n100
Supporting Variantsnssv3711828
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044946
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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