A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv679927



Internal ID15069893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:185445161..185586255hg38UCSC Ensembl
Innerchr4:186366315..186507409hg19UCSC Ensembl
Innerchr4:186603309..186744403hg18UCSC Ensembl
Innerchr4:186741464..186882558hg17UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38141095
hg19141095
hg18141095
hg17141095
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517035
Supporting Variants
Samples
Known GenesC4orf47, CCDC110, PDLIM3, SORBS2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv679927
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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