A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013100



Internal ID18755631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25256126..25354280hg38UCSC Ensembl
Innerchr1:25582617..25680771hg19UCSC Ensembl
Innerchr1:25455204..25553358hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3898155
hg1998155
hg1898155
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv133n100
Supporting Variantsnssv3475521
Samples
Known GenesRHD, TMEM50A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013100
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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