A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004074



Internal ID19093291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:177167037..177312111hg38UCSC Ensembl
Innerchr3:176884825..177029899hg19UCSC Ensembl
Innerchr3:178367519..178512593hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg38145075
hg19145075
hg18145075
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3614978
Samples
Known GenesLINC00501, TBL1XR1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1004074
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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