A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv682238



Internal ID15418890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:46079585..46136901hg38UCSC Ensembl
Innerchr22:46475465..46532781hg19UCSC Ensembl
Innerchr22:44854129..44911445hg18UCSC Ensembl
Innerchr22:44795984..44853300hg17UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3857317
hg1957317
hg1857317
hg1757317
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516279
Supporting Variants
Samples
Known GenesMIR3619, MIR4763, MIRLET7A3, MIRLET7B, MIRLET7BHG
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv682238
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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