A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv821372



Internal ID16063508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25258525..25338941hg38UCSC Ensembl
Innerchr1:25585016..25665432hg19UCSC Ensembl
Innerchr1:25457603..25538019hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3880417
hg1980417
hg1880417
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1420280
SamplesNA10851
Known GenesRHD, TMEM50A
MethodSequencing
AnalysisRead-depth of sequencing coverage was calculated for each base of human reference genome assembly build 36.3 (hg18) by our own script. Influence of GC contents on the read-depth of sequencing coverage was adjusted using modified method suggested by Yoon et al. We sought the relationship between GC contents and read-depth of coverage in 100bp windows. Then the single base RD (Read depth) was adjusted by the relationship.
PlatformIllumina IIx
Comments
ReferenceJu_et_al_2010
Pubmed ID20802225
Accession Number(s)nsv821372
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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