A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv692377



Internal ID15429029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:13122619..13142416hg38UCSC Ensembl
Innerchr18:13122618..13142415hg19UCSC Ensembl
Innerchr18:13112618..13132415hg18UCSC Ensembl
Innerchr18:13112618..13132415hg17UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3819798
hg1919798
hg1819798
hg1719798
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)nssv692377
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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