A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524665



Internal ID15451958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:36686570..36692791hg38UCSC Ensembl
Innerchr13:37260707..37266928hg19UCSC Ensembl
Innerchr13:36158707..36164928hg18UCSC Ensembl
Innerchr13:36158707..36164928hg17UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg386222
hg196222
hg186222
hg176222
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700634
Samples
Known GenesSERTM1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524665
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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