A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701107



Internal ID15437759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:156838512..156856404hg38UCSC Ensembl
Innerchr5:156265523..156283415hg19UCSC Ensembl
Innerchr5:156198101..156215993hg18UCSC Ensembl
Innerchr5:156198101..156215993hg17UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg3817893
hg1917893
hg1817893
hg1717893
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525058
Supporting Variants
Samples
Known GenesPPP1R2P3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701107
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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