A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523617



Internal ID15104224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:93027493..93066910hg38UCSC Ensembl
Innerchr15:93570723..93610139hg19UCSC Ensembl
Innerchr15:91371727..91411143hg18UCSC Ensembl
Innerchr15:91371727..91411143hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3839418
hg1939417
hg1839417
hg1739417
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699414
Samples
Known GenesCHD2, RGMA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523617
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