A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009868



Internal ID18752399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25269902..25346651hg38UCSC Ensembl
Innerchr1:25596393..25673142hg19UCSC Ensembl
Innerchr1:25468980..25545729hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3876750
hg1976750
hg1876750
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv141n100
Supporting Variantsnssv3482490, nssv3700623, nssv3463354, nssv3463628, nssv3700624, nssv3700622, nssv3476600, nssv3465053
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)nsv1009868
Frequency
Sample Size29084
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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