A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3481850



Internal ID18723238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25269444..25319681hg38UCSC Ensembl
Innerchr1:25595935..25646172hg19UCSC Ensembl
Innerchr1:25468522..25518759hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3850238
hg1950238
hg1850238
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1011563
Supporting Variants
Samples
Known GenesRHD
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3481850
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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