A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151349



Internal ID15879989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:220406407..220436051hg38UCSC Ensembl
Innerchr2:221271128..221300772hg19UCSC Ensembl
Innerchr2:220979372..221009016hg18UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg3829645
hg1929645
hg1829645
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv584505
Supporting Variants
SamplesNINDS_135
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151349
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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