A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005511



Internal ID18748042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25273802..25335709hg38UCSC Ensembl
Innerchr1:25600293..25662200hg19UCSC Ensembl
Innerchr1:25472880..25534787hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3861908
hg1961908
hg1861908
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv142n100
Supporting Variantsnssv3700628, nssv3476324
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)nsv1005511
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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