A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv958897



Internal ID15906167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:9892921..10042251hg38UCSC Ensembl
Innerchr3:9934605..10083935hg19UCSC Ensembl
Innerchr3:9909605..10058935hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg38149331
hg19149331
hg18149331
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589648
Supporting Variants
Samples
Known GenesCIDECP, CRELD1, EMC3, EMC3-AS1, FANCD2, IL17RC, IL17RE, JAGN1, LOC401052, PRRT3, PRRT3-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv958897
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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