A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517153



Internal ID15444446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:3220993..3222137hg38UCSC Ensembl
Innerchr11:3242223..3243367hg19UCSC Ensembl
Innerchr11:3198799..3199943hg18UCSC Ensembl
Innerchr11:3198799..3199943hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381145
hg191145
hg181145
hg171145
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv675400, nssv686735, nssv691935, nssv690175, nssv686525, nssv686974, nssv663182, nssv661398, nssv664391, nssv691896, nssv653880, nssv657526, nssv660952, nssv673665, nssv671168, nssv678413, nssv670992, nssv668330, nssv654771, nssv662420, nssv684729, nssv684541, nssv693027, nssv669467, nssv685029, nssv675050, nssv658292, nssv658653, nssv690931, nssv693427, nssv691579, nssv676371, nssv676654
Samples
Known GenesMRGPRG-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517153
Frequency
Sample Size2026
Observed Gain0
Observed Loss33
Observed Complex0
Frequencyn/a


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