A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001661



Internal ID18744192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:248461024..248550678hg38UCSC Ensembl
Innerchr1:248624325..248713979hg19UCSC Ensembl
Innerchr1:246690948..246780602hg18UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3889655
hg1989655
hg1889655
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv615n100
Supporting Variantsnssv3501005
Samples
Known GenesOR2G6, OR2T3, OR2T5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1001661
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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