A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv583527



Internal ID16370936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:163419425..163486179hg38UCSC Ensembl
Innerchr2:164275935..164342689hg19UCSC Ensembl
Innerchr2:163984181..164050935hg18UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3866755
hg1966755
hg1866755
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151324
Samples1780862404_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv583527
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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