A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522793



Internal ID15103400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:187966266..188141060hg38UCSC Ensembl
Innerchr4:188887420..189062214hg19UCSC Ensembl
Innerchr4:189124414..189299208hg18UCSC Ensembl
Innerchr4:189262569..189437363hg17UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38174795
hg19174795
hg18174795
hg17174795
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv332n21
Supporting Variantsnssv698437
Samples
Known GenesTRIML1, TRIML2, ZFP42
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522793
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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