A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516486



Internal ID15443779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:40132854..40146857hg38UCSC Ensembl
Innerchr13:40706991..40720994hg19UCSC Ensembl
Innerchr13:39604991..39618994hg18UCSC Ensembl
Innerchr13:39604991..39618994hg17UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3814004
hg1914004
hg1814004
hg1714004
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv669010, nssv692933, nssv681825, nssv687396, nssv680697, nssv668663, nssv705928, nssv682699, nssv704487, nssv682652
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516486
Frequency
Sample Size2026
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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