A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv711769



Internal ID15659039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25271785..25367695hg38UCSC Ensembl
Innerchr1:25598276..25694186hg19UCSC Ensembl
Innerchr1:25470863..25566773hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3895911
hg1995911
hg1895911
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545843
Supporting Variants
Samples
Known GenesRHCE, RHD, TMEM50A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv711769
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