A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv672106



Internal ID15062072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:74816295..74830515hg38UCSC Ensembl
Innerchr15:75108636..75122856hg19UCSC Ensembl
Innerchr15:72895689..72909909hg18UCSC Ensembl
Innerchr15:72895689..72909909hg17UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3814221
hg1914221
hg1814221
hg1714221
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520527
Supporting Variants
Samples
Known GenesCPLX3, LMAN1L
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv672106
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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