A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3486463



Internal ID19074104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:215279943..215356404hg38UCSC Ensembl
Innerchr1:215453286..215529747hg19UCSC Ensembl
Innerchr1:213519909..213596370hg18UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3876462
hg1976462
hg1876462
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003660
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3486463
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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