A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3635654



Internal ID18587249
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 StatusS
Merged Variantsnsv1031097
Supporting Variants
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)nssv3635654
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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