A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv904644



Internal ID15851914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:32760599..32827696hg38UCSC Ensembl
Innerchr2:32985666..33052763hg19UCSC Ensembl
Innerchr2:32839170..32906267hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3867098
hg1967098
hg1867098
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv581287
Supporting Variants
Samples
Known GenesLINC00486, TTC27
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv904644
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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