A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694489



Internal ID15084455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:150008925..150033472hg38UCSC Ensembl
Innerchr6:150330061..150354608hg19UCSC Ensembl
Innerchr6:150371754..150396301hg18UCSC Ensembl
Innerchr6:150422175..150446722hg17UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3824548
hg1924548
hg1824548
hg1724548
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517022
Supporting Variants
Samples
Known GenesRAET1L
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694489
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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