A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545998



Internal ID15986721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:36394151..36399101hg38UCSC Ensembl
Innerchr1:36859752..36864702hg19UCSC Ensembl
Innerchr1:36632339..36637289hg18UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg384951
hg194951
hg184951
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv712327
Samples
Known GenesLSM10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545998
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