A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000370



Internal ID19089587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161648141..161667408hg38UCSC Ensembl
Innerchr1:161617931..161637198hg19UCSC Ensembl
Innerchr1:159884555..159903822hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3819268
hg1919268
hg1819268
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv455n100
Supporting Variantsnssv3500406
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)nsv1000370
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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