A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563300



Internal ID16350709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:113162410..113163446hg38UCSC Ensembl
Innerchr13:113816724..113817760hg19UCSC Ensembl
Innerchr13:112864725..112865761hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381037
hg191037
hg181037
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv820486
Samples
Known GenesPROZ
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563300
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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