A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3473773



Internal ID18718950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25269444..25354280hg38UCSC Ensembl
Innerchr1:25595935..25680771hg19UCSC Ensembl
Innerchr1:25468522..25553358hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3884837
hg1984837
hg1884837
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1000794
Supporting Variants
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)nssv3473773
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