A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998666



Internal ID19158202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:158545091..158555833hg38UCSC Ensembl
Innerchr1:158514881..158525623hg19UCSC Ensembl
Innerchr1:156781505..156792247hg18UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg3810743
hg1910743
hg1810743
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv443n100
Supporting Variantsnssv3499301
Samples
Known GenesOR6Y1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998666
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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