A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv672532



Internal ID15409184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:46086105..46145351hg38UCSC Ensembl
Innerchr22:46481985..46541227hg19UCSC Ensembl
Innerchr22:44860649..44919891hg18UCSC Ensembl
Innerchr22:44802504..44861746hg17UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3859247
hg1959243
hg1859243
hg1759243
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)nssv672532
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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