A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703365



Internal ID15440017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:156838512..156856286hg38UCSC Ensembl
Innerchr5:156265523..156283297hg19UCSC Ensembl
Innerchr5:156198101..156215875hg18UCSC Ensembl
Innerchr5:156198101..156215875hg17UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg3817775
hg1917775
hg1817775
hg1717775
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526991
Supporting Variants
Samples
Known GenesPPP1R2P3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703365
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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