A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008812



Internal ID19098030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:186668886..186704337hg38UCSC Ensembl
Innerchr3:186386675..186422126hg19UCSC Ensembl
Innerchr3:187869369..187904820hg18UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3835452
hg1935452
hg1835452
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5003n100
Supporting Variantsnssv3615017, nssv3615016
Samples
Known GenesHRG
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1008812
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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