A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv914599



Internal ID6276526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:24163081..24997473hg19UCSC Ensembl
Outerchr22:24159620..25025810hg19UCSC Ensembl
Innerchr22:22493081..23327473hg18UCSC Ensembl
Outerchr22:22489620..23355810hg18UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1559902
SamplesMS24210
Known GenesADORA2A, C22orf13, C22orf36, C22orf45, CABIN1, DDT, DDTL, DERL3, GGT1, GGT5, GSTT1, GSTT2, GSTT2B, GSTTP1, GSTTP2, LOC284889, LOC391322, MIF, POM121L9P, SLC2A11, SMARCB1, SNRPD3, SPECC1L, SUSD2, UPB1
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv914599
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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