A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011005



Internal ID18753538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25269444..25361785hg38UCSC Ensembl
Innerchr1:25595935..25688276hg19UCSC Ensembl
Innerchr1:25468522..25560863hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3892342
hg1992342
hg1892342
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv140n100
Supporting Variantsnssv3700344, nssv3481389
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)nsv1011005
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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