A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997670



Internal ID19157207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161527110..161647837hg38UCSC Ensembl
Innerchr1:161496900..161617627hg19UCSC Ensembl
Innerchr1:159763524..159884251hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38120728
hg19120728
hg18120728
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv448n100
Supporting Variantsnssv3704747, nssv3501236
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)nsv997670
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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