A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525266



Internal ID15105873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:93027493..93058827hg38UCSC Ensembl
Innerchr15:93570723..93602056hg19UCSC Ensembl
Innerchr15:91371727..91403060hg18UCSC Ensembl
Innerchr15:91371727..91403060hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3831335
hg1931334
hg1831334
hg1731334
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv157n21
Supporting Variantsnssv701366
Samples
Known GenesCHD2, RGMA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525266
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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