A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002767



Internal ID19091984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161649018..161668711hg38UCSC Ensembl
Innerchr1:161618808..161638501hg19UCSC Ensembl
Innerchr1:159885432..159905125hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3819694
hg1919694
hg1819694
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv455n100
Supporting Variantsnssv3704805
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)nsv1002767
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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