A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998881



Internal ID18811731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:248534078..248647345hg38UCSC Ensembl
Innerchr1:248697379..248810646hg19UCSC Ensembl
Innerchr1:246764002..246877269hg18UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38113268
hg19113268
hg18113268
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv622n100
Supporting Variantsnssv3487374, nssv3485240, nssv3705593, nssv3705595, nssv3705592, nssv3705594, nssv3494478
Samples
Known GenesOR2T10, OR2T11, OR2T29, OR2T34, OR2T35
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998881
Frequency
Sample Size29084
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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