A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029535



Internal ID19118754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:30615616..30774562hg38UCSC Ensembl
Innerchr5:30615723..30774669hg19UCSC Ensembl
Innerchr5:30651480..30810426hg18UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg38158947
hg19158947
hg18158947
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3636025
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029535
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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