A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014951



Internal ID18757486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25269902..25351581hg38UCSC Ensembl
Innerchr1:25596393..25678072hg19UCSC Ensembl
Innerchr1:25468980..25550659hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3881680
hg1981680
hg1881680
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv141n100
Supporting Variantsnssv3478602
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)nsv1014951
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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