A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546852



Internal ID16334261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:94656962..94677287hg38UCSC Ensembl
Innerchr1:95122518..95142843hg19UCSC Ensembl
Innerchr1:94895106..94915431hg18UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3820326
hg1920326
hg1820326
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1173062
SamplesNINDS_196
Known GenesLINC01057
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546852
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer