A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525719



Internal ID15106326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:186490143..186599883hg38UCSC Ensembl
Innerchr4:187411297..187521037hg19UCSC Ensembl
Innerchr4:187648291..187758031hg18UCSC Ensembl
Innerchr4:187786446..187896186hg17UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38109741
hg19109741
hg18109741
hg17109741
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701882
Samples
Known GenesF11-AS1, FAT1, MTNR1A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525719
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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