A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582553



Internal ID16023276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:102061304..102074267hg38UCSC Ensembl
Innerchr2:102677765..102690727hg19UCSC Ensembl
Innerchr2:102044197..102057159hg18UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg3812964
hg1912963
hg1812963
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6981n54
Supporting Variantsnssv1151116
SamplesNINDS_196
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582553
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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