A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999000



Internal ID19158536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:143367483..143417286hg38UCSC Ensembl
Innerchr3:143086325..143136128hg19UCSC Ensembl
Innerchr3:144569015..144618818hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3849804
hg1949804
hg1849804
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3606126
Samples
Known GenesSLC9A9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999000
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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