A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561256



Internal ID16348665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:21154290..21155087hg38UCSC Ensembl
Innerchr13:21728429..21729226hg19UCSC Ensembl
Innerchr13:20626429..20627226hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38798
hg19798
hg18798
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv806192, nssv806191
Samples
Known GenesSKA3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561256
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer