A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014878



Internal ID19104095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:215279943..215354273hg38UCSC Ensembl
Innerchr1:215453286..215527616hg19UCSC Ensembl
Innerchr1:213519909..213594239hg18UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3874331
hg1974331
hg1874331
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv575n100
Supporting Variantsnssv3498184
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)nsv1014878
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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