A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014547



Internal ID19103765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161623061..161652367hg38UCSC Ensembl
Innerchr1:161592851..161622157hg19UCSC Ensembl
Innerchr1:159859475..159888781hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3829307
hg1929307
hg1829307
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3500290, nssv3498721, nssv3491324
Samples
Known GenesFCGR3B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014547
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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