A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561214



Internal ID16001937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:19837561..19877270hg38UCSC Ensembl
Innerchr13:20411701..20451410hg19UCSC Ensembl
Innerchr13:19309701..19349410hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg3839710
hg1939710
hg1839710
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv806052
Samples
Known GenesZMYM5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561214
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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