A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545927



Internal ID16333336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:30089416..30704226hg38UCSC Ensembl
Innerchr1:30562263..31177073hg19UCSC Ensembl
Innerchr1:30334850..30949660hg18UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg38614811
hg19614811
hg18614811
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv221n54
Supporting Variantsnssv712058
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545927
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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