A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007968



Internal ID18750499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:26687110..27108977hg38UCSC Ensembl
Innerchr3:26728601..27150468hg19UCSC Ensembl
Innerchr3:26703605..27125472hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg38421868
hg19421868
hg18421868
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3589562
Samples
Known GenesLRRC3B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007968
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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