A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv672899



Internal ID15409551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:13122619..13133578hg38UCSC Ensembl
Innerchr18:13122618..13133577hg19UCSC Ensembl
Innerchr18:13112618..13123577hg18UCSC Ensembl
Innerchr18:13112618..13123577hg17UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3810960
hg1910960
hg1810960
hg1710960
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515878
Supporting Variants
Samples
Known GenesCEP192
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv672899
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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