A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010402



Internal ID19099619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161642444..161668711hg38UCSC Ensembl
Innerchr1:161612234..161638501hg19UCSC Ensembl
Innerchr1:159878858..159905125hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3826268
hg1926268
hg1826268
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv454n100
Supporting Variantsnssv3483482, nssv3498389, nssv3499960, nssv3500858, nssv3493697, nssv3496617, nssv3488814, nssv3497283
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)nsv1010402
Frequency
Sample Size11257
Observed Gain5
Observed Loss3
Observed Complex0
Frequencyn/a


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