A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699435



Internal ID15089401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:186930134..188879332hg38UCSC Ensembl
Innerchr4:187851288..189800486hg19UCSC Ensembl
Innerchr4:188088282..190037480hg18UCSC Ensembl
Innerchr4:188226437..190175635hg17UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg381949199
hg191949199
hg181949199
hg171949199
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523635
Supporting Variants
Samples
Known GenesLINC01060, LOC339975, TRIML1, TRIML2, ZFP42
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699435
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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