A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515573



Internal ID15096180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:12172197..12184246hg38UCSC Ensembl
Innerchr11:12193744..12205793hg19UCSC Ensembl
Innerchr11:12150320..12162369hg18UCSC Ensembl
Innerchr11:12150320..12162369hg17UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3812050
hg1912050
hg1812050
hg1712050
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv663939, nssv682793, nssv682671
Samples
Known GenesMICAL2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515573
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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