A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563396



Internal ID16004119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:113802932..113820249hg38UCSC Ensembl
Innerchr13:114505905..114523222hg19UCSC Ensembl
Innerchr13:113590721..113608038hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3817318
hg1917318
hg1817318
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv820690
Samples
Known GenesGAS6-AS1, TMEM255B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563396
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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