A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000904



Internal ID19090121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:158376568..158441528hg38UCSC Ensembl
Innerchr3:158094357..158159317hg19UCSC Ensembl
Innerchr3:159577051..159642011hg18UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg3864961
hg1964961
hg1864961
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3606387
Samples
Known GenesRSRC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1000904
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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