A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031097



Internal ID18773630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:187304029..188382785hg38UCSC Ensembl
Innerchr4:188225183..189303939hg19UCSC Ensembl
Innerchr4:188462177..189540933hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg381078757
hg191078757
hg181078757
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635654
Samples
Known GenesLOC339975, TRIML1, TRIML2, ZFP42
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031097
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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