A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546822



Internal ID15987545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:93781021..93824307hg38UCSC Ensembl
Innerchr1:94246577..94289863hg19UCSC Ensembl
Innerchr1:94019165..94062451hg18UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg3843287
hg1943287
hg1843287
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv719302
Samples
Known GenesBCAR3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546822
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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