A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1154727



Internal ID15507532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:177357511..177469411hg38UCSC Ensembl
Innerchr5:176784512..176896412hg19UCSC Ensembl
Innerchr5:176717118..176829018hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38111901
hg19111901
hg18111901
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv600365
Supporting Variants
Samples1780862021_A
Known GenesDBN1, F12, GRK6, PFN3, PRR7, PRR7-AS1, RGS14, SLC34A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1154727
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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