A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002510



Internal ID19091727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:163773199..163922734hg38UCSC Ensembl
Innerchr1:163742436..163891971hg19UCSC Ensembl
Innerchr1:162009060..162158595hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38149536
hg19149536
hg18149536
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv457n100
Supporting Variantsnssv3501540
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)nsv1002510
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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