A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002256



Internal ID19091473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161532055..161652099hg38UCSC Ensembl
Innerchr1:161501845..161621889hg19UCSC Ensembl
Innerchr1:159768469..159888513hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38120045
hg19120045
hg18120045
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv448n100
Supporting Variantsnssv3501251
Samples
Known GenesFCGR2C, FCGR3A, FCGR3B, HSPA7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1002256
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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