A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014989



Internal ID19104206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:116377351..116390345hg38UCSC Ensembl
Innerchr3:116096198..116109192hg19UCSC Ensembl
Innerchr3:117578888..117591882hg18UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3812995
hg1912995
hg1812995
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4842n100
Supporting Variantsnssv3604470, nssv3604471, nssv3604472
Samples
Known GenesLSAMP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014989
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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