A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037571



Internal ID18780102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:100255653..100408741hg38UCSC Ensembl
Innerchr13:100907907..101060995hg19UCSC Ensembl
Innerchr13:99705908..99858996hg18UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg38153089
hg19153089
hg18153089
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525528
Samples
Known GenesPCCA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037571
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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