A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031129



Internal ID19120350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:7177225..7206432hg38UCSC Ensembl
Innerchr5:7177338..7206545hg19UCSC Ensembl
Innerchr5:7230338..7259545hg18UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3829208
hg1929208
hg1829208
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5559n100
Supporting Variantsnssv3639629
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)nsv1031129
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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