A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700106



Internal ID15436758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:26104451..26108873hg38UCSC Ensembl
Innerchr22:26500417..26504839hg19UCSC Ensembl
Innerchr22:24830417..24834839hg18UCSC Ensembl
Innerchr22:24824971..24829393hg17UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg384423
hg194423
hg184423
hg174423
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524218
Supporting Variants
Samples
Known GenesMIR1302-1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700106
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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