A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv665176



Internal ID15401828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:109301689..109333685hg38UCSC Ensembl
Innerchr4:110222845..110254841hg19UCSC Ensembl
Innerchr4:110442294..110474290hg18UCSC Ensembl
Innerchr4:110580449..110612445hg17UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3831997
hg1931997
hg1831997
hg1731997
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515893
Supporting Variants
Samples
Known GenesCOL25A1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv665176
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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