A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011650



Internal ID18754184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3797741..3934721hg38UCSC Ensembl
Innerchr3:3839425..3976405hg19UCSC Ensembl
Innerchr3:3814425..3951405hg18UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg38136981
hg19136981
hg18136981
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3739549
Samples
Known GenesLRRN1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011650
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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