A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546000



Internal ID15986723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:36459075..36495025hg38UCSC Ensembl
Innerchr1:36924676..36960626hg19UCSC Ensembl
Innerchr1:36697263..36733213hg18UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3835951
hg1935951
hg1835951
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1173814
Samples1780862529_A
Known GenesCSF3R, MRPS15
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546000
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