A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002184



Internal ID19091401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161642444..161667408hg38UCSC Ensembl
Innerchr1:161612234..161637198hg19UCSC Ensembl
Innerchr1:159878858..159903822hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3824965
hg1924965
hg1824965
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv455n100
Supporting Variantsnssv3483429, nssv3704801
Samples
Known GenesFCGR2B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1002184
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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