A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054527



Internal ID19143746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:68057325..68237516hg38UCSC Ensembl
Innerchr13:68631457..68811648hg19UCSC Ensembl
Innerchr13:67529458..67709649hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg38180192
hg19180192
hg18180192
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1702n100
Supporting Variantsnssv3527942, nssv3527943
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)nsv1054527
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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