A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998267



Internal ID19157804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:223446392..223472019hg38UCSC Ensembl
Innerchr1:223619734..223645361hg19UCSC Ensembl
Innerchr1:221686357..221711984hg18UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3825628
hg1925628
hg1825628
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3483949, nssv3705519
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)nsv998267
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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