A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3739549



Internal ID18691144
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 StatusS
Merged Variantsnsv1011650
Supporting Variants
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)nssv3739549
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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