A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525204



Internal ID15452497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:178680593..178748771hg38UCSC Ensembl
Innerchr4:179601747..179669925hg19UCSC Ensembl
Innerchr4:179838741..179906919hg18UCSC Ensembl
Innerchr4:179976896..180045074hg17UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3868179
hg1968179
hg1868179
hg1768179
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701286
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525204
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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