A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155926



Internal ID22086431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:232384437..232409435hg38UCSC Ensembl
Outerchr2:232378950..232415091hg38UCSC Ensembl
Innerchr2:233249147..233274145hg19UCSC Ensembl
Outerchr2:233243660..233279801hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg3836142
hg1936142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4016195
Samples
Known GenesALPP, ALPPL2, ECEL1P2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155926
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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