A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151837



Internal ID15534483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:37215767..37242920hg38UCSC Ensembl
Innerchr22:37611807..37638960hg19UCSC Ensembl
Innerchr22:35941753..35968906hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3827154
hg1927154
hg1827154
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv588987
Supporting Variants
SamplesNINDS_78
Known GenesRAC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151837
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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