A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv655312



Internal ID15045278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:185452162..185600889hg38UCSC Ensembl
Innerchr4:186373316..186522043hg19UCSC Ensembl
Innerchr4:186610310..186759037hg18UCSC Ensembl
Innerchr4:186748465..186897192hg17UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38148728
hg19148728
hg18148728
hg17148728
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517035
Supporting Variants
Samples
Known GenesCCDC110, PDLIM3, SORBS2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv655312
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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