A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698411



Internal ID15088377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:114829362..114830489hg38UCSC Ensembl
Innerchr2:115586939..115588066hg19UCSC Ensembl
Innerchr2:115303409..115304536hg18UCSC Ensembl
Innerchr2:115303169..115304296hg17UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg381128
hg191128
hg181128
hg171128
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522770
Supporting Variants
Samples
Known GenesDPP10
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698411
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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